Regulatory Affairs aspects of clinical trials and clinical Product Development in the EU 2016

Regulatory Affairs aspects of clinical trials and clinical Product Development in the EU 2016 is a seminar that covers topics such as:

• Pricing and reimbursement issues in your development
• Developing a regulatory strategy
• Scientific advice and how to choose between centralised and national scientific advice
• Orphan medicinal Products
• Advanced Therapy Medicinal Products
• Paediatric Investigation Plans
• Oncology medicinal products

Regulatory Affairs aspects of clinical trials and clinical Product Development in the EU 2016 brings together Regulatory Affairs personnel involved in Development of medicinal products.