Profile Summary
Tamil S.
5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...
Ilkay K.
20+ years of QMS experience, ISO 9001 Lead Auditor, ISO 14001, ISO 13485. Heading currently a team of MDR consultant in Germany and providing M...
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Johannes e g Hans V.
Eager to contribute with my passion for quality improvement, attention to detail, and auditing expertise, ensuring success process architecture...
Kristen H.
As a seasoned medical technical writer and chronic illness patient advocate, I am devoted to the meticulous translation of intricate medical in...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Khalaf A.
With a Bachelor of Science in Chemistry from King Saud University and a proven tenure as a Quality Director at Advance Medical Company, I posse...
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
Assaf G.
Medical devices professional with more than 25 years' experience in senior management positions in early stage medical device companies. A...
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Biomedical E.
Myself Umair Ahmed, a Biomedical Engineer and Scientist offering over 7 years of comprehensive experience in the freelance medical device consu...
Ali H.
Consulting services including application of IEC/EN 60601-1, IEC 62304, IEC 62366, ISO 14971. Project Management - Medical Devices Compliance. ...
Mohan M.
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...
Ayoub B.
I am a trilingual Biomedical Engineer (French/English/Arabic) with dual academic training from UTC Compiègne (France) and ENSAM Rabat (Mor...
Dr. Somnath Swami V.
Researcher with expertise in solubility enhancement and formulation development of pharmaceutical compounds, focusing on the use of mesoporous ...
Devin M.
I help medtech companies design, assess, and improve quality systems to ensure regulatory compliance, streamline development, and prepare for a...
Dr. Mohsen M.
I’m a biomedical engineer (PhD) with over 15 years of cross-functional experience in medical device development, neurotechnology, and regulator...
Dr. Alexandra A.
With 16 years of industry and academic experience combined in the medical device and interventional oncology fields, I am passionate about alig...
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Kathleen D.
👩🏻💼 Who I Am: Seasoned QMS and Compliance consultant dedicated to helping organizations achieve operational excellence...
Kristen D.
Innovative executive in clinical operations and regulatory affairs with successful experience in start-ups, hospital & CROs, private equity...
Mohamed H.
I am a Clinical Research Professional with over 13 years of global experience in clinical trial management, medical writing, and regulatory sub...
Woodrow S.
I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...
Dr. Diana K.
I’m a medical doctor (OB/GYN), bioinformatics & data science graduate, and experienced medical writer with 4+ years in clinical trial suppo...
Prafullakumar P.
I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...
Dr. Sevgi Ç.
14+ Years academic experience, expert in scientific writing, paraphrasing and biomedical documentation. Published author in SCI journals and b...
Dr. Patricia D.
I am a Pharmacist with a PhD in Sciences Applied to Health Products (UFF) and a Master’s degree in Pharmaceutical Sciences (UFRJ), combining ov...
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