A DYNAMIC CRO: STATE-OF-THE-ART MEDICAL TECHNOLOGY & REGULATORY COMPLIANCE HOW WE CAN HELP YOU The drug and device development world is a highly competitive market, where time is of essence. Any reduction in time needed to reach regulatory approval gives companies an edge over competitors. Thus, working with 1MED, a CRO that knows the ins and outs of pre-clinical and clinical research, development, and regulatory affairs, is of considerable strategic and economic benefit to your company. We stay up-to-date with leading industry practices, ISO standards, and regulatory changes from the European Medical Device Regulation (MDR). We also monitor developing regulatory trends to assist you at every stage of your drug or device life cycle. 1MED is a young company, founded in 2015, yet due to its knowledgeable team of experienced professionals, has over 40 years of experience in the life sciences. Our experience at 1MED in successful planning, clinical testing, regulatory approval, and bringing products to market, equips us with the skills and knowledge to properly advise you and help you achieve success. We can save you time, and therefore money, during the approval process for your medical device due to our predictable and stable costs. We handle a diverse array of projects in the medical device industry and offer support for all regulatory compliance issues worldwide. The repeat, long-term and diverse clientele we support speaks for itself; we are an added value to your company. We are not just another CRO, we are your collaborative proactive partner.