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In this video, our expert Jörg explores the crucial transition drug developers face when moving from laboratory research to clinical trials. As the focus shifts from the science of compounds to large-scale production, understanding how to manufacture an Active Pharmaceutical Ingredient (API) in a sterile environment becomes vital. He discusses the essential role of expert partners in this process, highlighting key aspects such as product formulation, sensitivities, handling methods and sourcing. Join us as we emphasize the importance of selecting the right Clinical Development and Manufacturing Organization (CDMO) to navigate these complexities, ensuring the successful transition from lab to clinic and safeguarding vital milestones in your clinical trials. -------------------------------------------------------------------------------------------------- Get more information on: our website: https://www.vetter-pharma.com/en/serv... LinkedIn: https://www. linkedin.com/company/vetter-pharma or subscribe to our newsletter: https://www.vetter-pharma.com/en/news... -------------------------------------------------------------------------------------------------- Click here to subscribe to our YouTube channel: / @vetterpharmaservices