Profile Summary
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...
Beliz A.
Bioengineer passionate about medical devices but even more loves to build meaningful, evidence-based relationships between medical devices and ...
Balaji C.
MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...
Madhu S.
• A competent Professional Medical Writer with over 7+ years' of experience in Regulatory Compliance, Quality Systems, Clinical Research, ...
Usman M.
Career Profile Regulatory Affairs Specialist with 5+ years of experience, in the creation and compilation of regulatory submissions to regulato...
Dr Febin F.
• Scientific Writer with experience in end-to-end handling of Clinical Evaluation Reports (CERs, both MDD and MDR compliance). • Authored scien...
Michal H.
Regulatory notifications under IVDD - Czech republic, Slovakia Regulatory notifications under MDD - Central Eastern Europe Regulatory registrat...
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...
Lini S.
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
Thelma A.
A pharmacist with over 6years of experience in the healthcare, medical device and pharmaceutical industry. Invested in carrying out research a...
Surya N.
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
Mahesh varma N.
Medical writing, Regulatory Writing, CER writing, Scientific consulting, Design, Biostatistics
Ashwini L.
Over 15 years of experience in Quality and Regulatory Affairs, Risk Assessment, Verification, and Validation, of medical devices like Patient M...
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...
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...
Soundarya P.
Handled more than 30 clinical evaluation reports end to end, starting from clinical evaluation plan, literature screening, literature summaries...
Caique M.
I am a freelance science and medicine writer, my focus is on implantable medical devices related to the areas of orthopedics. I specialized in ...
Kunle A.
I am a food scientist with 7years of experience. I have BSc in Food Technology and member Institute of Public Analyst of Nigeria (MIPAN). My e...
Kalidoss P.
Work experience in Medical device regulatory, cybersecurity of the medical device, clinical evaluation report analysis, risk benefit analysis.
Minh Tuan T.
Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...
Alexander B.
I have 12 years experience, starting as a Lead Coordinator at a clinical research site. Worked in the CRO space in study start-up, as a CRA, Cl...
Selina B.
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
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...
Regulatory 1.
* Expert knowledge on Medical Device, In-vitro Directive and Medical Device regulation in India * Qualified ISO Lead auditor, accomplished more...
Sachin M.
I am a medical device executive for last 20 years and have developed two innovative products, one nanotechnology based product among that. I ha...
Tarun S.
Medical device professional with strong background in single use disposables, reusable medical devices(Class I, Class II and Class III) . Broad...
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