Future of Medical Device Regulatory Affairs
Through the Complexity of everchanging regulations you need a partner to rely on
The Future of Medical Device Regulatory Affairs in IMEA
As healthcare spending continues to rise in India, Middle East and Africa (IMEA), the region has become a key growth target for medical device companies. One challenge faced by companies is overcoming the non-harmonised regulatory landscape which contains different systems, requirements and procedures.
Having a solid regulatory strategy in the region will require an in depth knowledge of the regulations and can open up a growing market. Using a combination of theory and practical case studies, Deliberate Consulting shares the knowledge needed to successfully navigate the medical device market in IMEA.
Future High Growth O&P Market
The Middle East Medical Device market is considered a manufacturer’s future high growth market. India, Pakistan, Saudi Arabia, UAE, Egypt, Turkey, and Israel are considered large markets in terms of size as well as in terms of payable capacity in the IMEA market.
From a Regulatory standpoint, most of the countries have their own systems in place, but at various stages of evolution. With a regional disparity in terms of accepting devices, the Middle East market seems a little complicated for importers and exporters to navigate through, for the purpose of medical device registration, but with the right guidance, this hurdle can easily be overcome.