Pharmaceutical Regulations Summit 2017

Topics

• 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

Who should Attend

Senior attendees with responsibilities in:

• Compliance
• Regulatory Affairs
• Market Access
• Registration
• Pharmacovigilance
• Labelling
• Drug Safety
• Quality Control
• Manufacturing