Consulting for Food, Drug and Medical Device Global Entries

With a focus on precision, efficiency, and foresight, we are committed to revolutionizing the journey of food, drug and medical device market entries through the seamless integration of strategic consultancy and unparalleled industry proficiency.

Regions we focus on

FDA Compliance

Navigating the regulatory landscape of the United States is paramount, and Mecca excels in meeting the rigorous standards set by the FDA. Our Regulatory Affairs team has extensive experiences in FDA requirements, ensuring that your products not only meet but exceed the expectations of this gold standard regulatory body.

CE Mark

For market access in the European Union, our Regulatory Insights experts facilitate the CE marking process. We understand the intricate requirements and nuances of European regulations, and our team ensures that your products comply with the essential health and safety requirements. Mecca acts as your strategic partner, guiding you through the CE marking journey with precision and expertise.

Device Clients 150+

Drug Clients 50+

Food Clients 100+