Pharmaceutical and Regulatory Training
Pharegistrum develops training tailored to companies’ needs. Topics can cover regulatory affairs, quality and scientific product knowledge, including preparation of materials for technical and commercial teams.
Training areas
- Regulatory affairs.
- Good Distribution Practices (GDP).
- Good Manufacturing Practices (GMP).
- ISO 13485.
- Medical Device and In Vitro Diagnostic Medical Device Regulations (MDR and IVDR).
- Advertising and promotional materials.
Topics are considered in the context of the company’s activities and identified needs. The programme, scope and conditions are defined in the training proposal.
Team training and supporting materials
Alongside technical and regulatory topics, Pharegistrum provides scientific and product training for commercial teams. Support includes the development of scientific or commercial training materials.
When describing your requirements, it is useful to distinguish between an introduction to a topic, more detailed coverage and support for a specific team need. This helps shape content around the objectives and participants’ knowledge.
Planning training for your company
Specify the topic, participant profiles and estimated numbers, learning objectives and team availability. If you already have materials or a reference programme, mention them in your request.
Contact us to discuss your needs and prepare a training proposal adapted to your organisation.
