Capability Building
Training life sciences teams to the standard the region's regulators expect
Regulatory, compliance, marketing, and safety teams are often trained on generic content that doesn't reflect market-specific frameworks. MSHealth delivers practical, market-specific training built on the same regulatory and pharmacovigilance work we run for our clients — not theoretical coursework.
Who this is for
Pharma and MedTech teams — regulatory affairs, compliance, medical, marketing, and pharmacovigilance functions — operating in or entering new markets, including staff who are new to the region's regulatory environment or need a structured refresher.
Training tracks
Four tracks, built for the region
Regulatory
Dossier requirements and submission procedures across MENA markets, including Morocco's AMMPS/DELM processes and EU MDR/IVDR requirements for MedTech products entering the region.
Compliance
CNDP and GDPR obligations for clinical and commercial data handling, GCP principles for teams involved in clinical research, and internal compliance frameworks appropriate to regional operations.
Marketing
Medical-legal-regulatory (MLR) review processes, promotional compliance for pharma and MedTech marketing, and the boundaries between scientific communication and promotional content under regional advertising codes.
Safety
Pharmacovigilance fundamentals — adverse event detection, case processing, signal management — and safety reporting obligations specific to MENA regulatory authorities.
Format
Modular workshops, on-site or virtual
On-site or virtual
Delivered in person at your location or remotely, at your pace.
Modular structure
Select one track or combine several to match your team's scope.
Certificate included
Each track closes with a certificate of completion.
Build your team to regional standard
Tell us which tracks your team needs and we'll send you a program outline.