Profile Summary
Dr. Diksha V.
I am a doctorate in life sciences with an experience of over 11 years in the academic and corporate sector. I have managed projects focusing o...
Madhu S.
Over 10 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, ...
Highly motivated Product Formulation Expert and Regulatory Affairs Expert in the following fields: Medical Devices ,Pharmaceuticals ,Dietary Su...
Adam F.
I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...
Joshita M.
A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...
Rudra P.
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
Bharti S.
A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...
Dr. Alex L.
Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...
Dr. Arinzechukwu U.
I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...
Dr. Sathesh Kumar A.
Fourteen years of R&D, Regulatory and Medical writing experience in various disciplines across In-vitro diagnostics, medical device regulat...
Dr. Grace C.
1. Clinical Evaluation Report (CER) writer and authoring of Clinical Evaluation Plan (CEP) in accordance with Medical Device Regulation (MDR), ...
Dr. Sandeep P.
Ph.D. in Chemistry having a total of 14+ years of experience in the pharmaceutical industry, expertise in the regulatory intelligence of pharma...
Dr. Mark P.
PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...
Dr. Trinadh Venkata Satish T.
Experienced Research Scientist with a Ph.D. and over 20+ years of demonstrated history of working in the areas of Tissue Engineering, Infectiou...
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Dr. Imen F.
PHD pharmacist, with more than 5 years of experience in Quality Assurance (QA) and Regulatory Affairs (RA). My experience enables me to help yo...
Dr. Samundeeswari M.
I’m a PhD chemist with 9+ years of research experience in fluorine chemistry and radioactive materials, now transitioning into regulatory affai...
Dr. Azza G.
Ph.D. trained clinician with expertise in bone biology, inflammation, and osseointegration. Established a career as a medical writer three year...
Dr. Sarah C.
Consultant to the digital health & life sciences industry with a strong research background in early stage drug discovery. I have extensive...
Dr. Waqar L.
Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...
Dr. Codette P.
Codette Pharma Regulatory Analytics Pvt Ltd provides top-level global regulatory and clinical support to Life Science companies. We are experts...
Dr. Nitin M.
After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...
Dr. Krutika G.
Here you can find more info:https://www.krutikagohil.com/ I am an award-winning professional digital health innovator. With my well-founded s...
Dr. Alpa B.
I am Dr. Alpa Ben, a BDS graduate from India. I have been working with healthcare service industry from past 8 years and have experience in var...
Dr. Vishal M.
Technology focused accomplished Material Scientist with research and professional expertise in developing innovative materials solutions. As a ...
Dr. Ankur P.
My expertise is development of clinical evaluation reports (CERs). This includes experience with literature searches, post-market surveillance,...
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EU MDR consulting services needed$550.00
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