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Quotient offers clinical trial manufacturing, testing and certification services to meet your requirements. We offer you manufacturing & testing services for major dosage forms such as solutions & suspensions, capsules, tablets etc.

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Clinical trial supplies manufacturing according to GMP (Good Manufacturing Practices) for pharmaceutical products for use in Phase I and II clinical trials.

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Bilcare GCS offers a wide range of clinical manufacturing capabilities to provide efficient and agile manufacturing of solid dosage, over encapsulation forms as well as liquids, creams, ointments, sterile dosage and aerosols.

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With dedicated GMP suites, laboratories and a clinical packing area, we are able to manufacture clinical supplies (packaged and labelled products) for trials around the world in a range of dosage forms.

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UPM provides cGMP manufacturing for clinical Phase I, II, and III products, including tablets, capsules and semi-solids. We are capable of producing batch sizes ranging from a few thousand units to over a million units per batch.

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Our contract pharmaceutical manufacturing services are cGMP compliant and include established clinical trial material and material management SOPs with QA oversight. In short, it meets your every clinical manufacturing need.

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Independent of your trial size and CTM demands, Ropack Pharma Solutions is equipped to meet your needs. Using QbD principles at each phase of scale, RPS ensures that all supplies are manufactured at the highest degree of quality.

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Custom Pharma Services has manufactured a wide range of solid dose, powders and hard gel capsules since 1979. Our facilities can manufacture existing and new formulations, providing innovative solutions for your hard-to-manufacture products. 250 million c

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Following the strong connection to the academic and innovative research, we are also certified for the manufacturing and packaging of Human Investigational Medicinal Products.

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Olive healthcare is a fully integrated developer, manufacturer and marketer of broad range of soft gelatin formulations with a strong regulatory and infrastructure back end to support its r&d and growth strategy in global markets.

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Aesica development centre is a purpose built facility which will specifically focus on formulation development and clinical manufacture. The development centre will also encompass all supporting analytical services and stability testing capability.