The Swiss-based company provides regulatory strategy, clinical trial management, and quality assurance services to support businesses through a product's lifecycle, from design and development to certification through regulatory, medical, preclinical, and clinical services. 1MED is ISO 13485:2016 certified and specializes in medical devices, including combination products, with a multidisciplinary and experienced team that can also support clients during the post-market life of their products. The company has a preferred partners network and consolidated relationships with European Notified Bodies and Competent Authorities, ensuring regulatory compliance while delivering tailor-made solutions that fit timing and budget needs.