Profile Summary
Shaheen Fathima A.
Regulatory documentation either moves a program forward or it doesn't. I make sure it does. I'm a RAC-Drugs certified Regulatory Affai...
Dr. Christoph P.
Most startups realize too late: getting a digital health product from concept to CE mark is as much a regulatory journey as a technical one. I...
Towanda L.
Regulatory Affairs: FDA submissions, EU MDR technical files, Post-Market Surveillance Reports (PSURs), and Declarations of Conformity. Quality...
Shivani A.
I am a Biotechnology professional with over 6 years of experience in clinical data management, regulatory documentation, scientific research, a...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
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Oliver S.
As a former Post-Market Surveillance & Vigilance Manager at Mathys (Swiss manufacturer of artificial joint implants), I have extensive hand...
Kamran V.
Expert in developing ISO 27001 Information Security, Penetration Testing, ISO 9001, ISO 14001, ISO 22000 Food Safety Management System, HACCP P...
Marianna C.
I am a Regulatory Toxicologist with a Master's degree in Pharmaceutical Sciences and postgraduate training in Industrial Toxicology, with p...
Mélodie K.
Executive leader in Quality, Regulatory, and Transformation Strategy, enabling life sciences organizations to accelerate market access, reduce ...
Deepa K.
I’m a passionate **Biochemistry postgraduate** with over **10 years of hands-on experience in Research & Development**, driven by a deep cu...
Dr. Amin J.
Biomedical Engineer (PhD) specializing in Medical Devices, Regulatory Writing, and Clinical Evaluation. Experienced in preparing CER, MDR‑compl...
David I.
I am a Medical Device Regulatory & Labeling Consultant and Founder of ATA Labeling Solutions LLC, specializing in global labeling complianc...
Dishan O.
I am a Mechatronics Engineer with expertise in biomedical engineering, artificial intelligence, computer vision, embedded systems, and medical ...
Dr. Lalit Raj S.
# Dr. Lalit Raj Singh **Medical Devices, IVDs & Pharmaceutical Regulatory Affairs | EU MDR/IVDR | WHO Prequalification | Technical Document...
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...
Karissa T.
I’m a seasoned Regulatory Affairs Consultant with over 17 years of experience supporting medical device and IVD companies in achieving global c...
Dr. Harriet K.
Regulatory writing and submissions • Regulatory Intelligence and Strategy Development • Toxicology Study Monitoring • Due Diligence and Gap Ana...
Dr. Jan S.
🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...
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Dr. Anushikha D.
I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...
Katerina S.
I am a Medical Physicist with over 20 years of clinical and research experience in radiotherapy, clinical trials, and medical device applicatio...
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Edwin M.
As a content writer, I craft compelling content that not only engages readers but also drives traffic. With a keen eye for detail and a deep un...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
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