Profile Summary
Madhu S.
• A competent Professional Medical Writer with over 7+ years' of experience in Regulatory Compliance, Quality Systems, Clinical Research, ...
Kavita S.
We are a team of experienced regulatory compliance expertise for Medical Devices and In-Vitro diagnostic devices across all risk classes. We ha...
Marin L.
Leading medical strategy in matrix-based global environment and providing scientific and business consultation to a local and global pharmaceut...
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Jose A.
Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Omnia T.
My name is Omnia and I am an Assistant Lecturer & Medical Writer with 6+ years of experience in the academic and professional sectors. I ho...
Arjun L.
I have a blend of experience in clinical medicine, pharmaceutical industry and medical device industry....As a medical doctor, I work on infectious diseases, pulmonary and critical care and public health....
Jessica H.
Global business leader seeking marketing healthcare consulting opportunities after working for companies including Micrus Endovascular, Johnson...
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...
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Mawaddi Q.
A clinical Evaluation specialist with clinical, research and occupational audiology background. I'm passionate in clinical research and any...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...
Haralabos P.
Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
Zahid R.
Highly motivated AI professional with over 3 years of experience in the field. Possessing a Master's degree in Computer Science and extensi...
Sammi D.
An experienced scientific and medical writer specialising in pharmacovigilance, medical communications and education currently working in the p...
Anuradha M.
I am post graduated in Pharmacy practice from National Institute of pharmaceutical education and Research,Mohali, India. I am a systematic revi...
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