Regulatory Affairs

At Adaptive Life Science, we pride ourselves on being the premier choice for recruiting support in regulatory affairs roles within the Medical Device, IVD, and Biotech industries. Our deep industry expertise, combined with a meticulous selection process, ensures that we connect our clients with highly qualified candidates who possess a minimum of three years to over forty years of relevant experience. By offering our services to candidates free of charge, we attract a diverse and talented pool of professionals, while our fee-based services for clients guarantee a tailored and dedicated recruitment experience. Trust Adaptive Life Science to provide authoritative and expert recruitment solutions that meet the stringent regulatory demands of your industry.

Digital Health

The Digital Health Sector is one of the fastest growing sectors within Healthcare, if not the fastest, and the global pandemic has only helped accelerate it.

Whether it’s a DiGA, new product coming to market, device utilizing AI or VR, we know them all and the companies offering innovation and creative freedom.

From VC backed start-ups to global players entering the digital health space, we have options to suit your style and product interests.

For our clients in digital health, we’re in contact with professionals across the wide spectrum of product management, from technical (with a track record of managing product development and design, including the planning process) to UX/UI, product growth and owners responsible for an entire app.

Traditional Medical Devices

Adaptive’s highly experienced consultants have grown an extensive network of top professionals and medical device manufacturers. We support product professionals with experience in all areas of the Medial Device space including Class I – III products, IVDs, Software, Invasive and Non-Invasive Devices, as well as Prosthetics and Implants.

Read Our Blogs

January 23, 2025

*EMA Update* Enhanced Access to Clinical Trial Information in Europe

The new version of the Clinical Trials Information System (CTIS) has been launched, providing earlier and more efficient access to clinical trial information in the European Union (EU) for patients, healthcare professionals, and other stakeholders. This improvement stems from revised transparency rules that have recently taken effect in Europe. The earlier availability of information about […]

December 10, 2024

The Evolution of Recruitment

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