The Pharmaceutical Regulatory Affairs in Latin America 2017 is a course that covers topics such as:
- The official regulatory information
- The requirements that underpin successful marketing authorisation appliations for pharmaceutical products across Latin America
- Hands-on experience in the region
- Interpretation and alternatives to local and specific legal requirements
- Requirements for the marketing of NCE, Biologic and biotechnology products, generic drugs and OTC medicines
- The regulatory aspects of site inspections
The Pharmaceutical Regulatory Affairs in Latin America 2017 brings together:
- Registration Departments
- Regulatory Affairs
- Analytical Research and Development
- Medical Directors
- New Business Development Departments
- Quality Assurance
- Regulatory Authorities