Part 8 cGMP - Product Management E-learning (asynchrone)

Objectives:

• Understand the procedures and responsibilities involved in the distribution of pharmaceutical products, particularly with regard to quality control and documentation. 

Topics covered:

Records and reports:

• General requirements
• Logbook for cleaning, maintenance, and use of equipment
• Records relating to medical devices, medical devices, and medications
• Batch records
• Distribution records
• Complaint records
• Key points

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.

• Multiple-choice assessment test
• Training certificate: yes
• Satisfaction survey

• 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: [email protected]

• Full cGMP process