Profile Summary
Dr. Ayesha M.
I am a qualified orthopaedic surgeon with over 6 years of clinical experience in trauma and fracture management, paediatric orthopaedics, defor...
Joy W.
I am a licensed oncology pharmacist and clinical researcher with over five years of hands-on experience in oncology clinical trials, pharmacovi...
Soutik D.
About Me I am a Regulatory Affairs professional with hands-on internship experience in the pharmaceutical sector, specializing in drug dossier ...
Khalil A.
Biomedical engineer and doctoral researcher (DBA) specializing in AI-enabled health technology assessment
Emilie M.
I am a freelance consultant with over 10 years of experience in regulatory affairs, specializing in Post‑Market Surveillance (PMS) and vigilanc...
Shashank M.
PROFESSIONAL SUMMARY GPAT-Qualified Research Professional with a Master of Pharmacy in Pharmacology and specialized expertise in C. elegans ani...
Rajesh K.
Take up projects in all areas of Quality and Regulatory of MedTech, Automotive and High Tech
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Jamila A.
I help MedTech companies bring regulated products to market — from early development through regulatory submission — with a particular focus on...
Jarrell M.
I am a medical device consultant with 25 years of experience helping companies bring products to market. I combine strong expertise in regulato...
Andrei L.
I bridge the gap between clinical requirements and advanced AI architecture. With a strong background in Healthcare & Medicine and deep tec...
Aradhana ..
Pharmacovigilance | Aggregate Safety Reporting | PBRER | PSUR | DSUR | Signal Detection | Signal Management | Benefit-Risk Assessment | Medical...
CASPAL O.
I am a Healthcare Data Analyst with a strong foundation in diagnostics, laboratory quality systems, and clinical data analysis, backed by forma...
Ashley K.
Regulatory Affairs and Quality Assurance specialist with nearly three years of hands-on experience supporting medical device and IVD manufactur...
Oskar S.
Regulatory affairs specialist with hands-on experience taking medical device manufacturers through the EU MDR transition. In my Quality & R...
Dr. Gaurav C.
Medical Advisor | Medical Affairs | Medical Writer | Medical Auditor | Healthcare Con 10+ years clinical experience; 8000+ cases; implants,
Dr. Dong Soo K.
About Me I am a Ph.D. Bioinformatician and Principal Investigator leading a Clinical Science Team in the oncology diagnostics industry. My expe...
Dr. Huda A.
I am a seasoned freelance translator working between Arabic, English, French, and Italian, with over 200 hours of simultaneous interpreting and...
Tomasz M.
MPharm and Statistical Programmer with 7+ years of experience in SAS, SQL, R, and Python, specializing in Real-World Data (EHRs, claims, survey...
Alicja Z.
Actor registration (SRN) and up to five device entries in EUDAMED, for manufacturers, importers and authorised representatives. Fixed written s...
Gabriela S.
I am a Regulatory Affairs and Quality Compliance professional with 7 years of experience across medical devices, in-vitro diagnostics (IVD), he...
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Chindu E.
Drug Data Analyst and Published Clinical Researcher (NIPER, M.Pharm) with expertise in pharmacovigilance, medical writing, regulatory affairs, ...
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Kay G.
Industry consultant/contractor with extensive hands-on experience assisting offshore and domestic clients in bringing molecules to market. Sub...
José Daniel C.
Biomedical Engineer, Microbiologist, and Master of Public Health (MPH) with over 5 yea...experience in the global medical device industry and healthcare public affairs....
Rita H.
I am a Regulatory Affairs and Quality Assurance consultant with 15+ years of experience in the medical device and pharmaceutical industries, an...
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