Ensure the success of your drug development program with Recipharm. We have the expertise and capability to support your drug development project from the early stages through to manufacturing.
Getting a drug product to market can be a challenging process with lots to consider, but Recipharm’s team of experts is here to support you.
Recipharm is a leading contract development and manufacturing organization (CDMO) headquartered in Stockholm, Sweden. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK, and the US and are continuing to grow and expand our offering for our customers.
We deliver a wide range of GMP-compliant services from our dedicated and flexible development facilities, and have been continually innovating and developing new technologies and processes for over 20 years.
A streamlined drug development process with input from experienced scientists is essential to avoiding pitfalls early in the drug development process and progressing a compound to the clinic. We take a holistic view when developing your product and give you access to a wealth of process development and production expertise that complements our manufacturing services.
Contact Recipharm today to discover how we can support you to achieve drug development success.