Profile Summary
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Obuchinezia A.
A dynamic and results-driven Medical Affairs Professional with extensive experience in conceptualising, developing, and managing international ...see more
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...see more
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...see more
Minh Tuan T.
Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...see more
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...see more
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. ...see more
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...see more
Pragatheeshwaran N.
Experienced in Medical device Post Market Surveillance (PMS) and process improvement. Familiarity with USFDA (21CFR Part 820, 806 and 803), QMS...see more
Sammi D.
An experienced scientific and medical writer specialising in pharmacovigilance, medical communications and education currently working in the p...see more
Anuradha M.
I am post graduated in Pharmacy practice from National Institute of pharmaceutical education and Research,Mohali, India. I am a systematic revi...see more
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication....see more
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...see more
Kolabtree is the leading online marketplace for Post-Market Surveillance experts. Post your project, get bids, and hire qualified experts quickly and easily.
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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