Suma Medtec

Suma Medtec can accelerate your development projects. Our personalized resources and solutions cater to medical device and pharmaceutical companies of all sizes. Check out our website for more information. Specialties: Medical Devices, Combination Products, New Product Development, Global Regulatory Affairs, Project Management, Design Controls, Risk Management and Usability, Quality Management Systems, Change Control, Audits, Submissions, Regulatory Strategy, ISO 13485, MDSAP, FDA, 510(k), De Novo, CE Marking | EU Authorized Representative, MDR, DHF, Design Verification, Design Validation.