FDA, EMA Requirements for New Drug Development and Generic Registration
The US and European Regulatory Processes for Generics
Key Developments in Market Exclusivity Requirements for Generic Authorisations
European and US Submission Strategies
Key requirements for Developments for Generic Authorisations
Who should Attend
Documentation Managers
Compliance Managers
Project Managers in Regulatory Affairs
Product Registration Personnel
Clinical Research Personnel
Marketing Managers
Key contributors to the submission package for the US and EU market
Past Events
Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics 2015 - 07-08 Jul 2015, The Rembrandt Hotel, London, United Kingdom (51378)
Important
Please, check "Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics" official website for possible changes, before making any traveling arrangements
