Hire a Medical Device Regulations Expert

I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...

I am a freelance science and medical writer catering to a diverse audience of scientists, healthcare professionals, pharmaceutical and medical ...

An accomplished, versatile, results-oriented clinical research professional with over 13 years of experience in the Pharmaceuticals & M...

I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...

A passionate lifelong student of Biomedical sciences with a Master’s degree from Carnegie Mellon University (CMU), I have always been fascinate...

Codette Pharma Regulatory Analytics Pvt Ltd provides top-level global regulatory and clinical support to Life Science companies. We are experts...

Mary Beth Ritchey, PhD, FISPE has spent more than 15 years in government, industry, consulting, and academia in better understanding medical pr...

1. Preparation of Clinical Evaluation Reports (CERs) in accordance with Medical Device Regulation (MDR) and 93/42/EEC Medical Device Directive ...

Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...

Scientific Writer with 9+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations ...

I am a pharmacist and a professional medical writer with over 11 years experience in various medical/pharmaceutical sectors including: researc...

I have more than 6 years experience (research and pharmaceutical industry) with a long track of success. My years as a researcher provided me ...

Authored medical device registration submissions (CERs) to international regulatory bodies (EU NBs) while ensuring regulatory compliance across...

I have a blend of experience in clinical medicine, pharmaceutical industry and medical device industry. As a medical doctor, I work on infectio...

I'm a therapeutic goods industry professional, working within the Australian medical device and pharmaceutical manufacturing sectors since ...

14 years of experience as an Electrical Engineer working in Medical Devices and Telecom for large organization and startups. * Drafting and rev...

20 years in Medical Devices, QA. RA, Validation for all Classifications of Medical Devices. MDR. IVDR expertise, with Software as a Medical Dev...

A self-motivated and committed Quality & Regulatory Affairs Professional with experience of working in the medical device sector in lin...

An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR, ISO-10...

A strong background in viorology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at hom...

* Ten years of writing experience in molecular biology, protein chemistry, cell biology and microscopy across three countries. * Six years of s...

Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...

I am medical writer with more than 5 years of experience in writing regulatory and clinical research document. My expertise is development of c...

Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...

My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...