Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Minh Tuan T.
Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
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...
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...
Eric D.
Over 25 years of experience in all facets of clinical research including with a focus on early phase medical devices and combination products. ...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
Anuradha M.
I am post graduated in Pharmacy practice from National Institute of pharmaceutical education and Research,Mohali, India. I am a systematic revi...
Sammi D.
An experienced scientific and medical writer specialising in pharmacovigilance, medical communications and education currently working in the p...
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