Pharmaceutical contract packaging service providers offer solutions for primary filling, primary packaging, secondary packaging, kitting services and folding cartons, applying their several years of experience in the contract packaging marketplace. Contract packaging facilities are equipped with fully dedicated and segregated capabilities for primary & secondary packaging of antibiotics like penicillin, cephalosporins, and carbapenemics, as well as oncological and sterile liquid dosage forms and other non sterile liquid formulations like syrup, suspensions with additional service of tamper evident sealing and Data matrix. For Customized Secondary Packaging, pharma companies assist with design and development of package, labeling and carton design or point-of-sale displays to provide market-appropriate usage information, whether distribution is to consumers, hospitals, physicians, short-run clinical trials, or wholesale groups. A flexible secondary packaging operation provides fully-integrated solutions for pharmaceutical packaging equipments and consumer product lines while maintaining strict compliance with cGMP and other FDA regulations. Some important Packaging and labeling services are Cartoning, Custom assembly, Clamshell blistering, Shrink-wrap bundling, Display assembly and packaging, Bagging and overwrapping, Kitting, Reworking, Carding, Hand assembly and inspection. A Contract goods packaging service provider can perform almost any secondary packaging operation, from simple cartoning, without insert, to the assembly of the most complex.

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Department of Packaging is a separate unit within Quinta-Analytica dealing with primary and secondary packaging in small scale of the solid dosage forms into blisters/strips or containers for research purposes, for clinical trials, and stability studies.

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Eurofins Contract Development & Manufacturing Organization offers GMP storage of 560 m3 at 15-25°C,146 m3 at 2-8°C, 2.6 m3 at 20°C and 0.5 m3 at -80°C.

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Development, manufacture and control of generic pharmaceutical specialties, both for Neuraxpharm and other laboratories, performed at Lesvi facilities in Sant Joan Despí (Barcelona), Spain

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Autajon is one of the main European leaders in the Set-up boxes, Packaging and Labelling industries. Autajon has international presence with a spirit of proximity

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Our range of single use passive bulk shipping solutions are suitable for all biopharma and clinical trial applications. Utilising advanced insulation to provide strict temperature control of your product within the demanding environment of global distribu

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Sharp’s clinical services division is one of the world’s leading providers of innovative clinical trial material supply chain services, with a talented and highly experienced team that can handle every aspect of your clinical trials project management.

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Rondo's experienced packaging engineers develop customised pharmaceutical packaging for clinical test samples, which combine a high degree of functionality, GMP compliance and patient compliance.

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Fisher Clinical Services runs the world’s largest clinical packaging operation. Fully owned facilities supporting ambient and refrigerated packaging are strategically situated around the globe to accommodate local or regional sourcing needs.

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Aphena provides independent, third-party services in packaging and randomization for clinical studies. Aphena comply with current Good Manufacturing Practices (cGMP) and Good Clinical Practices (GCP) regulations, standards and guidelines.

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Our Mecaplastic and Pentapack blister lines are equipped for various formats, enabling production of customized blister sizes, plus a camera inspection system for production traceability.

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Department of Packaging is a separate unit within Quinta-Analytica dealing with primary and secondary packaging in small scale of the solid dosage forms into blisters/strips or containers for research purposes, for clinical trials, and stability studies.

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Eurofins CDMO can perform customized labeling and secondary packaging of every clinical trial phases for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles).

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Creapharm & Sodia offers Manual and semi-automated bottling, Ability to handle many bottle sizes and types HDPE or glass, child-proof, desiccant, induction sealing.

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Fisher packaging facilities handle a range of package types including child-resistant blister cards and bottles, vials, patches, syringes, inhalers and other devices that contribute to the success of a clinical trial.

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At Sharp's state-of-the-art facilities, we design and print multi-language clinical labels for clients all over the world.

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Eurofins CDMO provides QP services including all the quality and regulatory support for clinical trial supplies. We can provide GMP certification, documentation review, audits of manufacturing sites, QP agreement, and final batch release.

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At Sharp we know that clinical studies are growing in complexity, with new geographic regions being introduced and fresh pressures on schedules, budgets and controls. That’s why our clinical packaging team does so much more than simply putting tablets in bottles.

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Our two sites comprise 14 independent suites, including one with an adjacent cold storage room dedicated to temperature-sensitive products. For products with a TOR 0 (Time Out of Refrigeration), all packaging operations are carried out at 2/8°C.

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As part of Fisher Clinical Services, Clintrak Clinical Labeling Services is the leading supplier of clinical labeling design, production and management services for the pharmaceutical and biotechnology industries.

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Eurofins CDMO can provide the primary packaging services of non-sterile solid forms (capsules, tablets) in HDPE bottles or blisters and in class C rooms. We provide a large range of bottles from 15 to 600mL with several options for caps.

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At Fisher's clinical services, Single & two panel labels can be manufactured in many sizes, on a variety of face-stock materials and base label adhesives to accommodate clinical trial materials for most application and storage conditions.

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Restricted area dedicated to designing and printing labels, leaflets and any other documents required. Close collaboration with our clients enables us to propose the most appropriate label design for each protocol and each type of patient kit.

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Servier CDMO offers a full range of contract development and manufacturing services, from concept and product development to analytical testing, commercial scale and regulatory approval.

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Eurofins CDMO can perform customized labeling and secondary packaging of every clinical trial phases for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles)

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Bilcare is at the forefront of delivering sustainable, affordable and innovative packaging solutions to customers globally. We follow a customer centric approach to fulfill packaging needs in the areas of pharmaceutical packaging, card solutions and specifications.

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Servier CDMO offers a full range of contract development and manufacturing services, from concept and product development to analytical testing, commercial scale and regulatory approval.