The Pharmaceutical Regulations Summit 2017 covers topics such as:
- Product registration and submission
- Current MENA and GCC regulatory landscape
- Harmonisation and standardisation of rules and guidelines
- Implementation of eCTD submission
- Market access, import/export and pricing
- Pharmacovigilance and post-market surveillance
- Global guidelines: European legislations and FDA perspectives
- Service delivery and usage
- Medical device regulations
The Pharmaceutical Regulations Summit 2017 brings together senior attendees with responsibilities in:
- Compliance
- Regulatory Affairs
- Market Access
- Registration
- Pharmacovigilance
- Labelling
- Drug Safety
- Quality Control
- Manufacturing