In international trade, in the last decades, tariff and customs barriers have been gradually reduced or eliminated, but a new barrier has gradually developed, the regulatory barrier set up for products that can have an impact on the health of citizens, such as Medical Devices and In Vitro Diagnostic Devices.
For manufacturers who want to export their products in all markets, orienting themselves in this maze of regulations and laws is really difficult.
Only an in-depth knowledge of all the legal requirements of each country can lead to an integrated and optimized path to effectively support the commercial strategy, and this is only possible for companies havin true "Regulatory Affairs" specialists on their payroll.
Maytal is able to offer to the MD and IVD manufacturers an outsourced "Regulatory Affairs" service, which integrates specialized and regulatory technical skills to allow companies, even the smallest ones, to build a path that allows to quickly achieve the marketing of products in the most important markets in the world.
