Founded in January 2020 and based in Horsham, United Kingdom. OMC is trusted by our clients for our service and transparency. During the uncertain period of Brexit, many of our clients were seeking a reliable partner to support them with the new UK regulations. OMC stepped up to fill this need and formed new relationships, which led to word-of-mouth referrals and collaborations with novel device manufacturers. We expanded our team and locations to meet the growing demand and established partnerships with like-minded organizations around the world. This allowed us to offer global regulatory support to our clients. We have built up a vast network of contacts to provide support for different regions, ranging from local registrations to local representatives. This network helps our clients gain market access and navigate the complex regulatory landscape.
Our motto is “breaking barriers for complex markets” and make the regulatory environment feasible to operate. We support our clients in all stages of product development, analyzing global strategy, implications and implementation of changes
At OMC, we are dedicated to breaking barriers and making regulatory environments feasible for complex markets. Our mission is to support our clients throughout all stages of product development, providing expert analysis of global strategies and guidance on how to implement changes effectively.
Our mission is to support our clients in launching their products in various markets, relieving them of complex procedures, and providing them with an effective regulatory strategy.
By ensuring our clients follow compliance, we want to support them with additional measures to ensure the device is safe for the end-user.
Our mission is to support our clients in launching their products in various markets, relieving them of complex procedures, and providing them with an effective regulatory strategy.
To empower medical device manufacturers with expert regulatory guidance, ensuring seamless compliance and uninterrupted supply chain operations, thereby safeguarding public health and advancing innovation in healthcare.
To be the premier partner in navigating the complex landscape of medical device regulations, renowned for our unwavering commitment to continuous compliance, excellence in service, and dedication to fostering a culture of innovation and safety in the healthcare industry.
We offer end to end solutions to address regulatory challenges, providing a comprehensive approach to compliance management.
Developing a strategic plan to ensure regulatory compliance and calculate ROI for product registration and market access across global markets.
Offering comprehensive registration and representation services to ensure smooth market access across various global markets.
Supporting with premarket and post market activities such as testing, validation, life cycle management and vigilance activities.
Streamline your license management effortlessly with effective support for registration and renewal services.
We take pride in offering a diverse range of language solutions to meet the global communication needs of businesses and individuals alike.
Your satisfaction is our priority, and our dedicated team is poised to assist you at every stage. Our team will be happy to respond to your queries. Contact us directly with your questions or schedule a FREE consultation, and we’ll be in touch as soon as possible.
Our team comprises experts from diverse fields of regulatory affairs and quality assurance. With a robust team, we offer worldwide assistance to our clients across multiple functions. Starting from medical device design requirements in compliance with relevant applicable standards, we assist in obtaining relevant certification or listings from the Ministry of Health (MoH). We also aid in introducing your devices to new markets and keeping product licenses up-to-date until the product reaches End of Service (EOS). Our specialization lies in regulatory affairs, where we provide comprehensive support for global regulations such as CE, FDA, UKCA, Med Do, CDSCO, and NMPA. Our services save valuable time spent on research and conflicting requirements, allowing our clients to streamline their regulatory processes and achieve compliance with ease.
Our mission is to support our clients in launching their products in various markets, relieving them of complex procedures, and providing them with an effective regulatory strategy.
By ensuring our clients follow compliance, we want to support them with additional measures to ensure the device is safe for the end-user.
Our mission is to support our clients in launching their products in various markets, relieving them of complex procedures, and providing them with an effective regulatory strategy.
We at OMC are thrilled and deeply honored to announce our feature in the historic and prestigious “75 Years of NHS” book, commemorating the illustrious history of healthcare in the UK. As we take a moment to reflect on our journey, we are filled with immense pride for the pivotal role we’ve played in shaping the health sector and contributing to the annals of Parliamentary history. Our unwavering commitment to supporting innovation, enhancing patient care, and collaborating closely with policymakers has been instrumental in placing us at the heart of this historic event, marking the transformative changes witnessed in the healthcare landscape over the past decades. Here’s to celebrating 75 years of dedication and progress by the NHS, and to the countless more years ahead dedicated to making a positive impact on healthcare! None of this would have been possible without the unwavering support of our esteemed clients and the tireless dedication of our exceptional team. We extend our heartfelt gratitude to our team for their relentless drive and to our clients for their trust and confidence in us to deliver on their requirements time and again. As we look to the future, we remain steadfastly dedicated to continuous improvement, ensuring that we continue to provide unwavering support to the NHS and our valued clients. Together, as we embark on the next 75 years, our goal remains clear: to leave an indelible mark in the annals of history through our contributions to healthcare.
Join us in celebrating this momentous occasion and in looking forward to the incredible journey ahead!
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
Our team will be happy to respond your queries. Contact us directly with your questions or for scheduling FREE consultation and we’ll be in touch as soon as possible.
To launch a medical device in a country, medical devices must comply with the local country’s regulatory requirements. Let us be your trusted partner in bringing your medical devices to the Global market. Contact us today to learn more about how we can assist you in every step of the way.
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