Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!
This course will show you how to write scientific documents such as a clinical evaluation in good and readable English that is appropriate to your audience, while complying with the regulatory requirements.
After this workshop, you will be familiar with organisational matters and best practice when writing, reviewing and ensuring the quality of your documents. Practical exercises and text review sessions will allow you to apply what you have learnt directly.
Marketing authorisation of medical devices in the GCC states like Saudi Arabia and the United Arabian Emirates, Egypt, Algeria, Morocco, Tunisia and Iran. This course gives you practical advice. Please take a look at the brochure.