Part 3 cGMP - Mastery of Raw Materials and Packaging Items
Dernière mise à jour : 28/10/2025
Description
Aucune description
Domaine : MEDICAMENTS, DM
Objectifs de la formation
Objectives:
- Understand regulatory requirements concerning the management of components and packaging items for formulated products.
- Learn how to identify, control, and ensure the quality of components and packaging items.
- Acquire the skills to assess and manage risks related to components and packaging items.
- Know how to implement procedures to ensure regulatory compliance and traceability of components and packaging items.
Public visé
Anyone involved in the production and control of medical devices. Human Resources, QMS Manager.
Prérequis
No prerequisites
Programme
Topics covered:
- Requirements, storage, and receipt
- Inspection and release
- Use of released raw materials (RM) and packaging materials (PM)
- Key points
Modalités pédagogiques
Interactive module consisting of expert videos, educational activities, etc.
Moyens et supports pédagogiques
Once you have placed your order, you will first receive an order confirmation email.
You will then receive confirmation of access to the module on our TREENING platform. This access is personal and secured by a password.
The TREENING Support Service is available to answer any technical or functional questions you may have.
If you have any questions specific to the module's subject matter, you can contact us via the discussion forum. One of our experts will respond as soon as possible.
At the end of your training, you will be invited to complete a satisfaction survey and, if applicable, download a training certificate.
Modalités d'évaluation et de suivi
- Multiple-choice assessment test
- Training certificate: yes
- Satisfaction survey
Infos complémentaires
- Module validity: 1 week after receipt of payment (extension possible)
- Training certificate: yes
- For orders of more than 10 modules, contact the training department for a personalized quote: tree@efor-group.fr