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We are a multi-service Contract Development and Manufacturing Organisation (CDMO), serving global pharmaceutical and biotechnology companies.
The extensive experience we gained working for over 20 years as part of one of the top 5 pharma companies has given us a unique insight into fulfilling client needs. Our wide range of services can support clients across the drug development pathway and includes expertise in drug substance synthesis and manufacturing scale up, drug product manufacture, bioanalytical services and radiolabelling synthesis.
We combine agility with flexibility to provide an innovative approach to the development and manufacture of pharmaceutical products. Our ambition is to save our clients valuable time, enabling them to rapidly bring life-changing medicines to market.
We help clients take their ideas for novel drugs through the clinical steps required to prove that a new medicine is effective and safe for use. Our state-of-the-art facility permits a wide range of specialist services for integrated end-to-end solutions. By combining services, we can remove the time delay caused by a large chain of suppliers. The teams at Arcinova are based on the same site, allowing them to efficiently work together to ensure that each drug substance or drug product passes through development stages quickly. We are also highly adaptable, providing bespoke services for customers who need to overcome specific challenges.
Our latest #CaseStudy describes the successful development of stable intravenous formulations for a chemically and physically unstable #API. Find out how the resulting IV formulations enabled a successful Phase I trial here: https://t.co/i9B4WSGgKy pic.twitter.com/omKVrTZEkK— Arcinova (@ArcinovaUK) January 21, 2020