Profile Summary
Mostofa Md G.
I am a Chemical Engineer and Formulation Chemist with extensive experience in research, product development, process optimization, and formulat...
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
William T.
Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...
Veer P.
A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...
Aida S.
I’m a PhD-trained medical writer and scientific strategist with 12+ years of experience spanning academic research, peer-reviewed publishing, i...
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. Ark K.
I am a PhD-qualified molecular biologist with over 20 peer-reviewed publications and scientific books. For the past 8 years, I’ve worked in the...
Dr. Umadevi R.
A Seasoned Medical Writer and Regulatory Affairs professional with a Ph.D. and extensive expertise in authoring high-impact clinical and regula...
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. Vipul G.
Interested in the application of the knowledge and skills acquired in Clinical Research and Clinical Data Management with data-interpretation s...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Violet S.
I am an EU MDR clinical evaluation specialist and RAC-Devices certified medical writer with over four years of experience developing Clinical E...
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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...
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...
Shivani A.
I am a Biotechnology professional with over 6 years of experience in clinical data management, regulatory documentation, scientific research, a...
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...
Kamran V.
Expert in developing ISO 27001 Information Security, Penetration Testing, ISO 9001, ISO 14001, ISO 22000 Food Safety Management System, HACCP P...
Dr. Amin J.
Biomedical Engineer (PhD) specializing in Medical Devices, Regulatory Writing, and Clinical Evaluation. Experienced in preparing CER, MDR‑compl...
Dr. Narimane K.
Pharmaceutical and biotech companies are increasingly adopting New Approach Methodologies (NAMs), yet many still face challenges in selecting t...
Dishan O.
I am a Mechatronics Engineer with expertise in biomedical engineering, artificial intelligence, computer vision, embedded systems, and medical ...
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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