Chromatography is widely considered the backbone of analytical chemistry testing within the FDA regulated industries. For instance, most compendial monograph methods for testing pharmaceutical products utilize some chromatographic techniques. Dietary supplements, in particular, are often comprised of a greater number of compounds and require significantly greater separation than pharmaceutical materials. It is necessary to leverage the power of chromatography to achieve the required separation. For these reasons, GPA retains a team of very experienced senior analysts who are very proficient in the use of our state-of-the-art chromatography instrumentation, including GC, GC-MS, HPLC, LCMS, and TLC. In Pharmaceutical sector, the main role is to identify and analyse samples for the presence of trace elements or chemical. Its major role is the separation of compounds based on their molecular weight and element composition. Chromatography also detects the unknown compounds and purity of mixture. Chromatography importance is growing its importance in drug development. HPLC and UPLC are both Liquid Chromatography used in separating the components of a compound or mixture. HPLC stands for High Performance Liquid Chromatography, and is a technique used to separate different constituents of a compound using high pressure to push solvents through the column. It is the most widely used technique to identify, quantify and separate components of a mixture. HPLC is widely used for the analysis of constituents of a pharmaceutical actives, drug products, pesticides, and countless other substances. In UPLC, or ultra-high performance liquid chromatography, column particle size of less than 2um can be used. This allows for better separation than the typical particle size of 5um that are used in HPLC. It also allows for a very fast analysis. Though, UPLC is a trademark technology it is used as a general term for this technique. Whereas the pump pressure in HPLC is 40MPa, in UPLC, this pressure can go up to 100MPa, which is what makes this technique so very exciting and efficient. GC is a technique for separating volatile substances by percolating a gas stream over a stationary phase. It is a technique that revolutionized analytical chemistry. GC has been applied successfully to numerous compounds in variety of fields. Headspace GC has been used since the 1980s, but only recently has it become part of mainstream of pharmaceutical analysis. TLC is known to have the best applications in Pharmaceutical Industry. They are largely used when it comes to the separation process. The use of pharmaceutical industry is gaining importance and there is huge success rates they are also delivering large number of medicines that are again challenging, but very few predictive scientific and analytical tools are available. Pharmaceutical industry tends to work on a regular pattern to improve the consistency of existing way so that they can match with the demands for best chemical measurements. In present days pharmaceutical analysis is largely dominated by expensive instrumental analysis.

- Service Details

Quinta is an established provider of multiple R&D and regulatory services for pharmaceutical, biotechnology and generic drug industries. Quinta holds GMP, GLP and GCP certificates.

- Service Details

Biondustria L.I.M's Central Quality Control Laboratory is located in Novi Ligure where finished products analysis are performed.

- Service Details

Our analytical centre provides these methods & equipment: Analytical methods and equipment are validated; LCMS, GCMS, HPLC, TLC; UV/VIS and IR spectrometry; Capillary electrophoresis; Thermal analysis – DSC, Calorimetry; NMR (400 MHz) + xRAY; PSD analysis

- Service Details

Well-equipped laboratories performing comprehensive tests for the finished products, WIP, raw materials, equipment cleaning in compliance to ICH guidelines using Pharmacopoeial methods, In-house test methods and customer's requirements.

- Service Details

HPLC & UPLC/UHPLC instrumentation with a wide variety of detection cap. (UV, DAD, RI, MS, MALS) to determine sample assay and purity of samples, along with quantitation for solubility, dissolution, diffusion and other techniques requiring quantitation

- Service Details

Our scientists perform routine quality control testing on thousands of our catalog products each year, giving them unparalleled expertise in developing and validating methods to analyze, quantify, and purify small molecules.

- Service Details

ScinoPharm's comprehensive analytical services include purity testing, characterization of polymorphs, analytic methods development and validation, as well as stability testing. All analytical instruments and data are managed through the company's Laboratory Information Management System

- Service Details

Zach has over 30 years of experience in multi-step syntheses involving complex reactions.We have dedicated R&D and analytical development teams on each site, and state-of-the art analytical equipment.

- Service Details

Softigel's seven cutting-edge facilities house a fully integrated PDS unit and covers all product life cycle phases from early development to commercial in the same plant, using equipment replication between non GMP and GMP.

- Service Details

Merck offers a wide range of very successful and innovative packing materials for HPLC, manufactured in the unique and easy-to-use LiChroCART® cartridge system with its manu-CART® holder.

- Service Details

ACTA Laboratories, Inc. is a cGMP FDA Registered Testing Laboratory that performs GC analyses on Pharmaceutical APIs (Active Pharmaceutical Ingredients) and Drug Products. ACTA can follow USP, BP, JP, and EP methods or develop methods of analysis for your API or Drug Product.

- Service Details

Our instruments and methods employ the most up-to-date innovations in technology and automation to perform analyses more efficiently and accurately. Frequently, modern instrumental analysis is the only way to accomplish assay determination of finished products.

- Service Details

We offer full compound certification and recertification services, which includes a comprehensive Certificate of Analysis, along with all supporting documentation.

- Service Details

Ultrasphere columns remain widely referenced within both industry and academia and are recognized to provide excellent chromatographic performance.

- Service Details

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.

- Service Details

Quinta is an established provider of multiple R&D and regulatory services for pharmaceutical, biotechnology and generic drug industries. Quinta holds GMP, GLP and GCP certificates.

- Service Details

Biondustria L.I.M's Central Quality Control Laboratory is located in Novi Ligure where finished products analysis are performed.

- Service Details

Zach has over 30 years of experience in multi-step syntheses involving complex reactions.We have dedicated R&D and analytical development teams on each site, and state-of-the art analytical equipment.

- Service Details

We have a R&D team working continuously on the development of formulas and pharmaceutical technologies. By combining new synthetic and natural substances with high-tech research equipment and new drug delivery systems, we offer differentiated products.

- Service Details

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.

- Service Details

ACE HPLC Columns offer unparalleled performance, excellent peak shape & guaranteed reproducibilit. ACE columns are available in eight bonded phases each offering a unique, and in some cases, dramatically different selectivity.