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Inside you will find
- What keynote speakers will be taking part in the exclusive speaking panel
- What Case Studies will be discussed by our senior corporate speakers
- The minute by minute breakdown of the conference
Conference Programme Overview
The 6th Annual Pharmaceutical Regulatory Affairs Summit programme is designed for senior pharmaceutical regulatory leaders, compliance specialists, pharmacovigilance experts and regulatory operations professionals.
The conference agenda will cover the latest FDA and EMA regulatory updates, AI in regulatory affairs, ISO IDMP implementation, global submission strategies, pharmacovigilance, eCTD management, regulatory intelligence and digital transformation within pharmaceutical compliance.
Attendees will gain practical insights into submission automation, global dossier management, evolving regulatory frameworks and emerging technologies shaping the future of pharmaceutical regulatory operations.
Who Should Attend
The summit is designed for Regulatory Affairs Directors, Regulatory Operations Managers, Compliance Specialists, Pharmacovigilance Leaders, Submission Managers, Quality Assurance Professionals and senior pharmaceutical executives involved in global regulatory strategy and compliance.
Key Topics Covered
- AI in Regulatory Affairs
- FDA and EMA Updates
- ISO IDMP Compliance
- Global Submission Strategies
- Pharmacovigilance and Drug Safety
- Regulatory Intelligence
- eCTD Submission Management
- Submission Automation
- Digital Transformation in Pharma
- Regulatory Data Governance