Profile Summary
Sonali S.
Having experience in medical device regulatory affairs, EUMDR, USFDA 510K, ISO 14971, ISO 13485
Peggy G.
Having over 20-years’ experience working in nursing and public health research, I turned my focus to medical writing almost a decade ago. I ha...
Puneet M.
MGCTS.ORG is a Contract Research Organisation that works for drug development across the world with major clients in Europe, Asia and Africa. W...
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...
Manas K.
20+ years of planning, developing, executing, managing global strategic upstream marketing initiatives including developing roadmaps for portfo...
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...
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Marin L.
Leading medical strategy in matrix-based global environment and providing scientific and business consultation to a local and global pharmaceut...
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...
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....
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Megha B.
I have 15+ years of experience in health economics and outcomes research (HEOR) and market access in the US and globally. I have prepared healt...
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. ...
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...
Jessica H.
Global business leader seeking marketing healthcare consulting opportunities after working for companies including Micrus Endovascular, Johnson...
Mawaddi Q.
A clinical Evaluation specialist with clinical, research and occupational audiology background. I'm passionate in clinical research and any...
Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
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Obuchinezia A.
A dynamic and results-driven Medical Affairs Professional with extensive experience in conceptualising, developing, and managing international ...
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
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...
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
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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