Profile Summary
Dr. Paula P.
- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...
Dr. Nadeem A.
• Cell biologist with seven years of academic scientific writing experience • MBA candidate in Medical Devices and Healthcare Management with t...
Dr. Karim E.
I hold a Ph.D. in Biological Sciences from the Université Libre de Bruxelles (ULB), Belgium, specializing in gene therapy against cancer. ...
Dr. Eric L.
With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...
Dr. Sonia C.
I have been working for the health industry, In-vitro diagnostic and medical devices for over 20 years, mainly at R&D positions and alw...
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
Selina B.
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
Pradip F.
I am managing R & D project for in-vitro diagnostics, in-vitro drug screening, medical device, and vaccine development. I look into all as...
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...
Michal H.
Regulatory notifications under IVDD - Czech republic, Slovakia Regulatory notifications under MDD - Central Eastern Europe Regulatory registrat...
Manas K.
20+ years of planning, developing, executing, managing global strategic upstream marketing initiatives including developing roadmaps for portfo...
Lakshman Prakash B.
Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...
Jacqueline V.
Registered healthcare professional with 16 years of clinical experience in academic hospitals and clinical research. Trained in Clinical Evalua...
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Akhthar S.
Sr. Executive & Entrepreneur with experience in Biotech, SaaS Healthcare, Medical Devices, Biomaterials- Cellulose, fibers, starch, PHA, PB...
Sarah B.
I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Kristen H.
As a seasoned medical technical writer and chronic illness patient advocate, I am devoted to the meticulous translation of intricate medical in...
Khalaf A.
With a Bachelor of Science in Chemistry from King Saud University and a proven tenure as a Quality Director at Advance Medical Company, I posse...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
ADNAN A.
20 years in Medical Devices, QA. RA, Validation for all Classifications of Medical Devices. MDR. IVDR expertise, with Software as a Medical Dev...
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
Dr. Loleta R.
Seasoned clinician innovator (MD, MBA) and data-driven strategist with unique healthcare and business acumen. Proficient in leading in-depth ma...
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...
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