Part 6 cGMP - Laboratory Controls
Dernière mise à jour : 28/10/2025
Description
Aucune description
Domaine : MEDICAMENTS, DM
Objectifs de la formation
Objectives:
- Identify the various obligations and responsibilities of laboratories in terms of quality control.
- Learn how to implement and document laboratory control procedures that comply with cGMP.
- Recognize the importance of verification, calibration, and maintenance of laboratory equipment.
Public visé
Anyone involved in the production and control of medical devices. Human Resources, QMS Manager.
Prérequis
No prerequisites
Programme
Topics covered:
- General requirements
- Controls and release for distribution
- Stability studies
- Specific requirements
- Reserve samples
- 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