Iso Life Sciences

ISO Life Sciences understands the business and technical challenges of Medical Devices Regulation and Compliance. We offer proprietary analytical tools and methods to rapidly and accurately assess the MDD to MDR compliance gaps and have the technical and business consulting expertise to help design and implement accelerated solutions. ISO Life Sciences' experiences in Medical Devices Regulation and Compliance have taught us that, although guided by RA, the MDD requires a business led solution involving all functions and almost inevitably including a strategic review of product portfolios. Success requires a combination of Business Transformation and Technical and Clinical expertise underpinned by Programme Design that embraces Change Management. We can provide comprehensive programme design and execution and this is most effective when we work in close collaboration with cross-functional teams from your organisation. ISO Life Sciences was formed by partners with extensive experience of the Med Tech and Consulting world. We have UK, EU and US based resources and, with our strategic alliance partners can support analyses and implementations for global and geographically dispersed clients. We have an enviable track record in our employees and associates who have worked to respond to the many diverse changes required of today's MedTech sector.
Social Link - Linkedin: http://www. linkedin.com/company /iso-lifesciences
Employee Count: 2
Keywords: 3rd party contract management