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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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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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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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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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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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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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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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Capsugel-Tampa offers complete primary and secondary packaging services in support of a broad spectrum of clinical projects including worldwide distribution, storage, and logistics under climate-controlled conditions, and clinical retains, returns, accountability, reconciliation, and destruction.

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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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At PCI we combine knowledge, experience, and innovative technologies to provide our customers packaging services that ensure safety and reliability throughout.

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PCI's primary packaging capabilities feature scalable options to meet the varying needs of each trial, from small Phase I studies to the largest Phase III and Phase IV programs.

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We offer tailored clinical manufacturing services to ensure a successful launch of your clinical trial. We develop your product according to your technical requirements within your timeframe.

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Bluepharma performs its activity from product development to the end of the value chain, that is, finished product supply.