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API Development
Analytical Method Development
Analytical Testing Services
BioAnalytical Services
Biologic Drugs
Biologics, Bioprocess & Fermentation
Clinical Development / Phase IIb-IV
Compliance, Regulatory & Consulting
Container Closure Integrity
Continuous Flow Process
Contract Manufacturing
Custom Synthesis & Manufacturing
Early Clinical / Phase I-IIa
Fine Chemical / Intermediate
Formulation Development
Hospital Supplies / Medical Disposables
Injectable / Parenteral
Lyophilization
Packaging and Distribution Testing
Patient / Investigator Recruitment
Post Marketing
Preformulation & Material Science
Process Development & Optimization
Protein / Peptide
Reference Standard
Rx / OTC & Orphan Drug Products
Separation & Purification
Serialization Equipment
Small Scale Batch
Stability Studies
Sterile APIs
Technology / Data / Analytics
AES Life Sciences
Dalton Pharma Services
Neopharm Labs Inc
Nutrasource
Optel Vision
Phyton Biotech LLC
Verity Pharmaceuticals Inc
WellSpring
CANADA
Canada
World’s Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Phyton Biotech is the World's Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Pharma Service: API Manufacturing
Category: Biologics, Bioprocess & FermentationSub Category: Overview
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Our product testing division offers full analytical services for active ingredient characterization, potency and a wide range of ingredient-specific analyses.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: High Potency APIs (HPAPIs)
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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The Manual Print Station™ is a completely manual station for printing and verification of cartons, ensuring accurate serialization identification.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Labelling & Printing - Manual
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The Verity Pharma commercial and medical team monitors and studies the Canadian pharmaceutical landscape. It is currently bringing specialty pharmaceuticals that are well entrenched in treatment protocols and in demand by physicians, for their patients.Th
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Pharma Service: Sales, Marketing, Registration
Category: Rx / OTC & Orphan Drug ProductsSub Category: Canada
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Complete Pharmacopoeial / Compendial Testing
World’s Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Phyton Biotech is the World's Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Pharma Service: API Manufacturing
Category: Contract ManufacturingSub Category: Overview
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At Nutrasource, we offer a variety of testing services to provide your firm with the necessary qualifications for a CoA for your product.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Overview
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The CLTracker TE™ handles the printing and verification of each carton and ensures accurate serialization identification.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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The Verity Pharma commercial and medical team monitors and studies the Canadian pharmaceutical landscape. It is currently bringing specialty pharmaceuticals that are well entrenched in treatment protocols and in demand by physicians, for their patients.Th
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Pharma Service: Sales, Marketing, Registration
Category: Hospital Supplies / Medical DisposablesSub Category: Canada
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
World’s Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Phyton Biotech is the World's Leader in Plant Cell Fermentation Technology and Commercial Manufacturing.
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Pharma Service: API Manufacturing
Category: Custom Synthesis & ManufacturingSub Category: Overview
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Chromatography (TLC / LC / HPLC / UPLC / GC)
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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Pharma Service: Analytical
Category: Container Closure IntegritySub Category: Assessment Programs
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Our product analytics division offers full analytical testing services to ensure your products and ingredients comply with regulatory requirements for quality and purity.
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Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Method Development and Validation
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The PackStation™ FMP is a complete manual packing station that ensures the identification and verification of manually packed products with bar code scanners.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Labelling & Printing - Manual
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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The PackStation™ SAP is a semi-automated packing station that ensures the identification and verification of manually packed products with cameras.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Semi-Automatic Inspection / Verification
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: FTIR / NIR
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We have a dedicated stability and analysis group at our laboratory, Diteba, providing comprehensive support for all stages of drug development, including early research and development to commercial or post-approval studies.
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TrackSafe™ ables you to do serialisation and aggregation with focus on the preservation of the performance of your packaging lines and your overall equipment effectiveness (OEE).
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Our in-house Diteba laboratory provides a wide range of physical testing services, including:Loss on Drying, Moisture (Karl Fisher Titration and Coulometric),Color Determination, Container/Closure Integrity, Deliverable Volume etc.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Physical Characterization
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Physical Characterization
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: UV Spectrophotometry
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The LabelTracker™ is a complete automated station, such as a Labeler, that allows the identification and verification of unit level products for serialization.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Dissolution
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Our skilled and competent Chemistry group uses a wide range of methods to test raw materials, FDFs and packaging components in accordance with compendial procedures including but not limited to: USP/NF, BP, Ph. Eur, JP, CP, FCC, ACS, AOAC, AOCS, In-house and client supplied methods.
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Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Impurity Isolation and Identification
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Our facilities and testing methods are compliant with all Health Canada, FDA, USP and other regulatory body requirements and guidelines in order to provide effective testing services for your product.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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To ensure your product complies with the regulations, we offer testing for most metals via ICP-MS equipment providing very low detection limits.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Trace / Elemental / Heavy Metals
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The BottleTracker™ ensures the printing and inspection of a unique temporary identifier on Bottle bottom for fast product and tracking code association with the ability to reject and re-insert Bottles.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Labelling & Printing - Automatic
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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The True Anisidine Value (TAV) test, a proprietary analytical method developed by Nutrasource scientists, solves a common issue faced by the omega-3 industry: false-positive rancidity readings in coloured and flavoured marine oils.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Overview
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The Flying CartonTracker™ is an ultra compact unit that handles the printing and verification of cartons with the ability to reject any single carton on the fly. The Flying CartonTracker™
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Stability StudiesSub Category: Photostability
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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We offer method development, validation and specimen analysis using state-of-the-art laboratory equipment and techniques, including Ultra Performance Liquid Chromatography Mass Spectrometry (UPLC/MS/MS) and liquid and gas chromatography techniques.
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Pharma Service: Analytical
Category: BioAnalytical ServicesSub Category: Overview
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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Our scientists at WellSpring have years of experience using advanced analytical equipment to ensure precision during all our testing procedures. Our facility is fully equipped with modern chemistry and microbiology laboratories that operate beyond cGMP standards.
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Pharma Service: Analytical
Category: Packaging and Distribution TestingSub Category: Shelf Life and Accelerated Aging Testing
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The BundleTracker™ ensures the identification of products within a Bundle by creating the child/parent relationship.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Limited documentation with older products has the potential to hinder a smooth transfer. Historical experience for the product may not be available as the product to be transferred may be an acquisition of an old product, but the existing site should be willing to share whatever experience
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Pharma Service: API & Drug Product Development
Category: Formulation DevelopmentSub Category: Tech Transfer
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The PackStation™ (CAP) is a completely automated packing station that allows the identification and verification of both products and containers with cameras.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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Our in-house laboratory, Diteba, offers analytical services in:Method development, validation and method transfer for Potency assay, Related substances (impurities), Dissolution methods; Forced degradation studies; and Cleaning validation testing.
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Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Overview
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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The PalletMaster™ allows the idenfication and verification of both cases and pallets with cameras and/or bar code scanners for central palletizing area.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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When performing a site-to-site transfer, personnel with the knowledge and experience of the product must assist in the transfer training, guidance and assessment for the internal receiving site.
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Pharma Service: API & Drug Product Development
Category: Formulation DevelopmentSub Category: Tech Transfer
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Participant enrollment is often the single largest cause of delays in clinical research and often accounts for one quarter of the clinical program timeline. Our team expedites this process by taking a strategic approach to clinical trial recruitment.
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Pharma Service: Clinical Trials
Category: Patient / Investigator RecruitmentSub Category: Patient Recruitment
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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Our regulatory team stays abreast of ever changing regulations in the North American market. Our clients have diverse portfolios often crossing different regulatory categories.
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Pharma Service: Clinical Trials
Category: Compliance, Regulatory & ConsultingSub Category: Regulatory Affairs
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To be successful, the receiving entity must demonstrate to the satisfaction of the regulatory bodies both the knowledge and the capabilities to perform the critical elements of the transfer.
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Pharma Service: API & Drug Product Development
Category: Formulation DevelopmentSub Category: Tech Transfer
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The CartonTracker™ handles the printing and verification of each carton and ensures accurate serialization identification. Optel’s TrackSafe™ solution addresses product authentication and traceability requirements in the pharmaceutical industry.
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Pharma Service: Packaging
Category: Serialization EquipmentSub Category: Automatic Inspection / Verification
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Pharmaceutical Water
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Unlike other CROs that often provide a one-size-fits-all approach to statistical analysis, Nutrasource offers a flexible approach to biostatistics driven by your clinical research goals.
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Pharma Service: Clinical Trials
Category: Technology / Data / AnalyticsSub Category: Clinical Biostatistics and Programming
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We have a speciality in early phase trials involving healthy volunteers. Early phase trials may have many factors that must be considered to achieve the research goals.
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Pharma Service: Clinical Trials
Category: Early Clinical / Phase I-IIaSub Category: Phase I / IIa
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Method Development and Validation
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At Nutrasource, we combine clinical expertise in the areas of nutrition, nutraceuticals and pharmaceuticals, as appropriate, to manage trials efficiently and effectively to support product investigations in support of a successful product launch.
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Pharma Service: Clinical Trials
Category: Clinical Development / Phase IIb-IVSub Category: Phase II / III
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Particle size
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Our Clinical Research Associates (CRAs) are an extension of our Sponsors. They are experienced at working effectively with sites to ensure patient recruitment and study execution goals are met.
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Pharma Service: Clinical Trials
Category: Technology / Data / AnalyticsSub Category: Clinical Trial Monitoring
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
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Our regulatory team stays abreast of ever changing regulations in the North American market. We take the stress out trying to understand the differences in regulations, classification and requirements between Canada and the United States.
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Pharma Service: Clinical Trials
Category: Compliance, Regulatory & ConsultingSub Category: Regulatory Affairs
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All analyses are performed in compliance with cGMP requirements using methods from relevant compendia and pharmacopoeia. Our experienced microbiology team can perform a wide range of compendial assays, including: USP/NF, AAMI, BP/Ph. Eur, AOAC, AWWA, FDA-BAM and Client supplied methods.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Physical Characterization
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As part of our mission of ensuring sound scientific evidence in support of safe and effective products, our team places emphasis on product safety. We offer our clients a flexible suite of pharmacovigilance services during product development.
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Pharma Service: Clinical Trials
Category: Post MarketingSub Category: Pharmacovigilance / Product Lifecycle Management
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Neopharm has two distinct validation departments; chemistry and microbiology. Each validation department is dedicated to development, validation, verification, recovery and inter-laboratory transfer of analytical methods.
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Pharma Service: Analytical
Category: Packaging and Distribution TestingSub Category: Shelf Life and Accelerated Aging Testing
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Through Diteba, we offer method development, validation and specimen analysis using state-of-the-art equipment and techniques. These include Ultra Performance Liquid Chromatography Mass Spectrometry (UPLC/MS/MS) as well as liquid and gas chromatography.
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Pharma Service: Analytical
Category: BioAnalytical ServicesSub Category: Overview
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Our team understands that upfront planning is critical for the success of every clinical trial and that planning must be produced in cooperation with your clinical team.
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Pharma Service: Clinical Trials
Category: Early Clinical / Phase I-IIaSub Category: Phase I / IIa
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Neopharm has two distinct validation departments; chemistry and microbiology. Each validation department is dedicated to development, validation, verification, recovery and inter-laboratory transfer of analytical methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Dissolution
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Neopharm has two distinct validation departments; chemistry and microbiology. Each validation department is dedicated to development, validation, verification, recovery and inter-laboratory transfer of analytical methods.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Residual Solvents
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Nutrasource is staffed with a qualified team including physicians, nurses and certified clinical coordinators. Extensive clinical trial experience in food, dietary supplement and pharmaceutical research, ensuring delivery of highest quality results.
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Pharma Service: Clinical Trials
Category: Technology / Data / AnalyticsSub Category: Clinical Trial Monitoring
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Neopharm offers a full range of stability testing and storage services to meet the performance needs of our clients. Our stability operations include 15,000 cubic feet of walk-in/reach-in chambers/incubators that meet the ICH guidelines requirements.
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Pharma Service: Analytical
Category: Packaging and Distribution TestingSub Category: Shelf Life and Accelerated Aging Testing
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Neopharm offers a full range of stability testing and storage services to meet the performance needs of our clients. Our stability operations include 15,000 cubic feet of walk-in/reach-in chambers/incubators that meet the ICH guidelines requirements.
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Pharma Service: Analytical
Category: Stability StudiesSub Category: Photostability
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Neopharm offers a full range of stability testing and storage services to meet the performance needs of our clients. Our stability operations include 15,000 cubic feet of walk-in/reach-in chambers/incubators that meet the ICH guidelines requirements.
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Advanced Electrophoresis Solutions Ltd. (AES) is located in Canada’s Technology Triangle. It is dedicated to providing the life science industry the most reliable, highest performance, and highest throughput whole column imaging detection for protein purity testing by Capillary Electrophoresis.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Capillary Electrophoresis
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Dalton is a leader in the sterile cGMP manufacture of aseptically filled or terminally sterilized liquid parenteral vials. Batch sizes range from 100’s of vials up to 15,000 vials per batch.
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Pharma Service: Drug Product Manufacturing
Category: Injectable / ParenteralSub Category: Overview
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Dalton uses its upgraded sterile filling room to aseptically fill the vials and then transfers them to our fully programmable cGMP lyophilizer. Our lyophilization batch sizes can range from 6936 vials (2 ml vial configuration) to 680 vials
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Advanced Electrophoresis Solutions Ltd. (AES) is located in Canada’s Technology Triangle. It is dedicated to providing the life science industry the most reliable, highest performance, and highest throughput whole column imaging detection for protein purity testing by Capillary Electrophoresis.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Capillary Electrophoresis
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Dalton offers high quality lyophilization services which include cycle optimization and cGMP production for clinical scale batches.
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Pharma Service: Drug Product Manufacturing
Category: Injectable / ParenteralSub Category: Overview
- Service Details
Advanced Electrophoresis Solutions Ltd. (AES) is located in Canada’s Technology Triangle. It is dedicated to providing the life science industry the most reliable, highest performance, and highest throughput whole column imaging detection for protein purity testing by Capillary Electrophoresis.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Capillary Electrophoresis
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Dalton specializes in cGMP sterile powder filling into vials. Our unique capability allows us to fill neat sterile powders with suitable flow characteristics into vials in a Class A (100) environment.
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Pharma Service: Drug Product Manufacturing
Category: Injectable / ParenteralSub Category: Overview
- Service Details
AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for biosimilars.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
- Service Details
Dalton offers a selection of in-stock vial container closure options and commonly used excipients to deliver your aseptic clinical materials faster in full compliance.
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Pharma Service: Drug Product Manufacturing
Category: Injectable / ParenteralSub Category: Clinical Supply
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AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for biologics.
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Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
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Dalton offers the manufacturing of sterile cGMP APIs by a variety of methods including sterile filtration and dry heat sterilization. Our sterile product manufacturing capabilities include sterile filling of powders, liquids and lyophilization.
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AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for recombinant proteins.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
- Service Details
AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for peptides.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Small Scale BatchSub Category: Overview
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
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Pharma Service: API Manufacturing
Category: Continuous Flow ProcessSub Category: Overview
- Service Details
AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for antibody drug conjugates.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Process Development & OptimizationSub Category: Overview
- Service Details
AES is a capillary electrophoresis service provider, It is dedicated for providing protein separation, quantification, and characterization. It also offers capillary electrophoresis method development for monoclonal antibodies.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Method DevelopmentSub Category: Capillary Electrophoresis
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Custom Synthesis & ManufacturingSub Category: Route Scouting
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Custom Synthesis & ManufacturingSub Category: Route Scouting
- Service Details
Statistical Design of Experiments (DoE) for process parameterization and optimization
- Directory Listing
Pharma Service: API Manufacturing
Category: Process Development & OptimizationSub Category: Overview
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Separation & PurificationSub Category: Extraction & Isolation
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API Manufacturing
Category: Separation & PurificationSub Category: Extraction & Isolation
- Service Details
Dalton Pharma Services is an ideal contract partner for your API Process Development. We are FDA registered and Health Canada approved, and provide integrated process development, API manufacturing and finished dose manufacturing at a single location.
- Directory Listing
Pharma Service: API & Drug Product Development
Category: Preformulation & Material ScienceSub Category: Polymorph & Crystal Screening
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Dalton’s Custom Synthesis and Fine Chemical services offers a wide range of experience in the synthesis of low volume, high value small molecules for biotechnology and pharmaceutical applications.
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Pharma Service: API & Drug Product Development
Category: API DevelopmentSub Category: Custom Synthesis
- Service Details
Dalton’s Custom Synthesis and Fine Chemical services offers a wide range of experience in the synthesis of low volume, high value small molecules for biotechnology and pharmaceutical applications.
- Directory Listing
Pharma Service: API Manufacturing
Category: Fine Chemical / IntermediateSub Category: Overview
- Service Details
Dalton’s Custom Synthesis and Fine Chemical services offers a wide range of experience in the synthesis of low volume, high value small molecules for biotechnology and pharmaceutical applications.
- Directory Listing
Pharma Service: API Manufacturing
Category: Fine Chemical / IntermediateSub Category: Overview
- Service Details
Dalton’s Custom Synthesis and Fine Chemical services offers a wide range of experience in the synthesis of low volume, high value small molecules for biotechnology and pharmaceutical applications.
- Directory Listing
Pharma Service: API Manufacturing
Category: Reference StandardSub Category: Overview
- Service Details
Dalton can provide material in a range of peptide purity from 70-98%. Mass spectrometry is used to verify the mass of the peptide.
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Pharma Service: API Manufacturing
Category: Protein / PeptideSub Category: Synthesis
- Service Details
Dalton Pharma Services is a recognized leader in offering custom Conjugation Services as a tool for Drug Delivery, Targeted Drug Delivery, Synergistic Drug and Gene Delivery, or Diagnostic applications.
- Directory Listing
Pharma Service: Drug Product Manufacturing
Category: Biologic DrugsSub Category: Antibody Drug Conjugate
- Service Details
Dalton Pharma Services can perform screening of polymorphic forms for any API of interest via state of the art analysis including DSC, XRPD, FTIR and dissolution/solubility testing to determine the best polymorphic form for your product.
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Pharma Service: API & Drug Product Development
Category: Preformulation & Material ScienceSub Category: Polymorph & Crystal Screening
- Service Details
With over 2,000 high quality research molecules in our catalogue, Dalton has over 30 years of expertise in structure elucidation of unknown synthetic impurities, intermediates, degradants, and excipient-related impurities.
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Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Structure Elucidation
- Service Details
Identification of Unknown impurities of >0.05% abundance using internally developed or client supplied method.
- Directory Listing
Pharma Service: API & Drug Product Development
Category: API DevelopmentSub Category: Impurity / Reference Standard
- Service Details
Identified compounds can be ultra-purified for use as reference standards for QC analysis and stability impurity monitoring studies.
- Directory Listing
Pharma Service: API & Drug Product Development
Category: API DevelopmentSub Category: Impurity / Reference Standard
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Light Microscopy
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Karl Fischer / Water Analysis
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Particulate Matter
- Service Details
Dalton offers a full range of microbiology testing services to support every product need.
- Directory Listing
Pharma Service: Analytical
Category: Analytical Testing ServicesSub Category: Microbiology
- Service Details
Dalton supports its customers' products with our in-house stability services including full stability services from protocol development for accelerated stability, intermediate term stability and long term stability programs.
- Directory Listing
Pharma Service: Analytical
Category: Packaging and Distribution TestingSub Category: Shelf Life and Accelerated Aging Testing
- Service Details
Dalton supports its customers' products with our in-house stability services including full stability services from protocol development for accelerated stability, intermediate term stability and long term stability programs.
- Service Details
Dalton supports its customers' products with our in-house stability services including full stability services from protocol development for accelerated stability, intermediate term stability and long term stability programs.
- Service Details
Dalton supports its customers' products with our in-house stability services including full stability services from protocol development for accelerated stability, intermediate term stability and long term stability programs.
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