EU Regulatory Affair’s

2^nd International Conference and Exhibition on Pharmaceutical Regulatory Affairs

November 23-24, 2012 Hyderabad International Convention Centre, India

Nagesh Maddula

Scientific Tracks Abstracts: Pharmaceut Reg Affairs

Abstract :

Background to regulatory affairs The European legislative framework Marketing Authorisation Applications Labels and leaflets European Procedures Lifecycle management, including variations

Biography :

Nagesh Maddula: Nagesh is owner and Director of Regulatory Affairs for Biovision Consultants Ltd. He is a Pharmacist with MS in Biotechnology. He has extensive experience of supporting the global pharmaceutical industry to achieve product development and regulatory approvals worldwide. He has been involved with scientific advice procedures, and product registrations.