Learn how CRO/CDMOs successfully address operational and regulatory challenges for pharmaceutical and biotechnology clients; and how this can make the difference between study success or failure.
In this webinar we will reveal the inner workings of the manufacturing and pharmacy department of a CRO/CDMO, so you understand the different regulatory and operational considerations faced by a clinical research pharmacy.
You will learn about inherent challenges, and the appropriate mitigation measures and optimization solutions that deliver the most effective results and outcomes.
What will you learn?
• Study planning, including quantity calculation, and how to minimize deviations
• Safely and successfully working with Schedule I products
• Packaging and labeling requirements for different countries and jurisdictions
• Shipping and importation logistics during the COVID-19 era
Who may this interest?
• Small pharmaceutical startups
• Pharmaceutical companies
• University research department heads