Author: omcmedical

OMC Medical Limited stands as a trusted UK Responsible Person for medical devices, playing a pivotal role in ensuring compliance with post-Brexit regulatory requirements. As the UK evolves its regulatory... Read More

OMC Medical Limited facilitates the CDSCO (Central Drugs Standard Control Organization) registration process, ensuring seamless market entry for medical products in India. With a deep understanding of CDSCO regulations, OMC... Read More

OMC Medical Limited facilitates seamless cosmetics registration in South Africa, ensuring compliance with regulatory standards. With expertise in navigating registration processes, they prioritize safety and quality assurance. Trust OMC Medical... Read More

OMC Medical Limited specializes in facilitating the registration process for medical devices in Iraq, ensuring compliance with local regulations. With comprehensive expertise, they guide manufacturers through documentation, submission, and approval... Read More

OMC Medical Limited pioneers streamlined license transfers for medical devices to new local Authorized Representatives (AR) in New Zealand. Our innovative approach ensures regulatory compliance and expedites market entry, empowering... Read More

Regulatory services in China and compliance with the EU Medical Device Regulation (MDR) are critical for companies like OMC Medical Limited. Operating in a global market, navigating the intricacies of... Read More

Compliance in post-marketing surveillance is paramount for OMC Medical Limited to ensure product safety and regulatory adherence. Monitoring adverse events, product complaints, and ensuring timely reporting to regulatory authorities are... Read More

OMC Medical Limited navigates the process of medical device registration in the United Arab Emirates (UAE) with precision and compliance. Understanding the significance of regulatory approval, OMC diligently follows the... Read More

Unlocking worldwide opportunities for healthcare innovation, OMC Medical Limited pioneers Global Market Access Strategies for Software as a Medical Device. Seamlessly navigating regulatory landscapes, we ensure our software meets international... Read More

The Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte), BfArM, is the institution responsible for regulating medical devices in Germany. Headquartered in Bonn, BfArM operates under... Read More