Meet our team at the RAPS Euro Convergence, the most comprehensive regulatory affairs conference in Europe, focusing on the latest developments in healthcare products in Europe and beyond—medical devices, IVDs, pharmaceuticals, and combination products. BSI Speakers: Alex Laan, Sara Fabi Register >...
Health Canada Regulatory Services Services that help make the drug and health product regulatory process more manageable, predictable and successful. Regulatory Services Regulatory submissions and life cycle management of drug, medical device and other health products for Canada. ...
Cosmereg regulatory affairs consultants assist clients to comply with the US FDA, Health Canada and EU regulations for cosmetics, food, medical devices and dietary supplements industries.
Theresa has over 30 years’ experience working in both the Pharmaceutical and Medical Device industries and has worked in a variety of roles across the full development cycle from product concept and early-stage development, process transfer, validation and regulatory departments. In addition to her...
Medical device, pharmaceutical, and biotechnology companies frequently hire medical writers or medical journalists. The nature of writing can vary from company to company. Medical writers are mainly involved in the preparation of regulatory documents, scientific documentation, and documentation during clinical...
📑 About Freyr Life Sciences: Freyr Life Sciences is the largest global Regulatory Solutions & Services provider, supporting Life Sciences companies of all sizes—pharmaceutical, medical device, and biotech—in navigating the complexities of regulatory compliance. As a fast-growing and innovative compan...
Syneos Health | Associate Director, Regulatory Strategy | montréal, qc 📑 DescriptionRegulatory Affairs Associate DirectorSyneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial ...
Medical Technologies, Tuv Sud Canada Inc., medical devices,electrical safety,orthopedics,certifcn/testing,ce marking,regulatory affairs,testing,, Canada Medicaltech
Clinical Operations have a lot of interaction with people in a range of other departments includingClinical Science, Clinical Quality Assurance, Data Management, Biostatistics and Regulatory Affairs to ensure that the data and information needed by these other departments is delivered so they can decide...
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