Profile Summary
Usman M.
Career Profile Regulatory Affairs Specialist with 5+ years of experience, in the creation and compilation of regulatory submissions to regulato...
Viqar A.
Nanotechnology and Medical Device enthusiast with experience in New Product Development, Regulatory Affairs and Quality Management System. Work...
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...
Dr Febin F.
• Scientific Writer with experience in end-to-end handling of Clinical Evaluation Reports (CERs, both MDD and MDR compliance). • Authored scien...
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...
Marysa M.
Marysa is a Medical Device Regulatory Consultant with over six years’ experience executing clinical-regulatory documentation and demonstrated k...
Lini S.
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
Damla V.
Hi, I have almost 15 years of experience in a multinational Pharmaceutical and Medical Device company as a QA/RA manager. My Specialties -Exp...
Thelma A.
A pharmacist with over 6years of experience in the healthcare, medical device and pharmaceutical industry. Invested in carrying out research a...
Lakshman Prakash B.
Experience in Lifesciences industry including over 18 years’ experience in QA, QMS, Regulatory, Manufacturing, Quality Unit (Commissioning, Qua...
Tasmiatul K.
1. Registered and Licensed Pharmacist (RPh) in Bangladesh (Reg. No- A 4845) 2. Experienced Professional equipped with skills in the field of Re...
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Jacqueline V.
Registered healthcare professional with 16 years of clinical experience in academic hospitals and clinical research. Trained in Clinical Evalua...
Akhthar S.
Sr. Executive & Entrepreneur with experience in Biotech, SaaS Healthcare, Medical Devices, Biomaterials- Cellulose, fibers, starch, PHA, PB...
Surya N.
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
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...
Sarah B.
I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...
Mahesh varma N.
Medical writing, Regulatory Writing, CER writing, Scientific consulting, Design, Biostatistics
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....
Peter O.
Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...
Viktoria K.
I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...
Tamil S.
5 years experience as an Quality Assurance professional.I have a broad background, topics include: - ISO 13485:2016 - 21 CFR 820 - ISO 14971, ...
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. ...
Ramamurthy J.
▪ Writing, reviewing quality and ensuring timely delivery of CEP/CER, PMSP/PMSR/PSUR to the client according to EU-MDR/MDD regulations and rela...
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