Medical Device Regulations in the Middle East

29-Jul-2014

27 October 2014, Seminar, Raffles Hotel, Dubai, UAE

27 October 2014

Seminar

Raffles Hotel, Dubai, UAE


This seminar will provide an essential overview of the key areas of requirements for product approvals for medical devices in the Middle East. The programme will cover the regulatory requirements and developments in the individual countries.

Organiser: Management Forum

Featured Companies

Related Content

Biological Evaluation of Medical Devices
Biological Evaluation of Medical Devices
Medical Device Summer School: From concept to CE marking
Medical Device Summer School: From concept to CE marking
Pre-filled Syringes - Advances in Manufacture
Pre-filled Syringes - Advances in Manufacture
Device/Drug and Drug/Device Combinations in the EU and USA
Device/Drug and Drug/Device Combinations in the EU and USA
The Role of the Qualified Person under the Medical Device Regulations
The Role of the Qualified Person under the Medical Device Regulations
Usability and human factors engineering
Usability and human factors engineering
Injectable Drug Delivery
Injectable Drug Delivery
Design, development and performance evaluation of medical devices
Design, development and performance evaluation of medical devices
FDA Medical Device Inspections
FDA Medical Device Inspections
Isolators, Barriers and Containment Technology
Isolators, Barriers and Containment Technology