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Munich: Biopharmaceutical Development and Manufacturing: Developing Tomorrows Medicines and Technologies –

• On 18 – 19 June 2009, Dr. Hiltrud Horn will give a two day- training course on “Development of Biotech Products and Advanced Therapy Medicinal Products (ATMPs) - Regulatory and GMP Aspects -”
• Day 1 will focus on clinical trials and IMPD. Her presentation will cover various aspects of how to compile, organise and word successfully IMPDs in order to minimise delays during the review process.
• Day 2 will focus on the CTD, Interaction with Authorities, ATMPs. Dr. Horn will present the relevant issues of the regulatory and GMP aspects within the scope of the CMC development of biotech and ATMPs.

For more information please visit the following website:
http://www.pda.org/MainMenuCategory/GlobalEventCalendarandRegistration/European-Events/Development-of-Biotech-Products-and-Advanced-Therapy-Medicinal-Products-ATMPs-Regulatory-and-GMP.aspx

(Conference organized by PDA)

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