Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics 2015 is a conference that covers topics such as:
- 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
Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics 2015 brings together:
- 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