When your focus is on growing your international business, you don’t want to be limited due to a lack of skilled resources in your QA/RA team. Is your team struggling to meet expected registration process timelines? Do you face issues with your document management? Many of our clients have a challenge to find sufficient, experienced, regulatory talent.

Important updates to the India Medical Equipment registration and importation process

In this blog we will go into more detail on the Medical Device Marketing Authorization (MDMA) and the role of the Authorized Representative

Over the past years we have seen an enormous growth in foreign direct investments in India, whereby foreign companies like Siemens,...

The Egyptian Drug Authority (EDA) has recently published an update to the Egyptian registration process for Medical Devices and IVD.

Gateway MedTech offers a total project management solution, through local expertise, resources and network.