Profile Summary
Lais C.
I executed: project 1: Brazil and Mexico, conversations between cultures; Project 2: Teaching Genetics in Schools project 3: sustainable entrep...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
George B.
I have a strong track record of conducting systematic reviews, as evidenced by my numerous co-authorships (simply search for 🔍Burchell ...
Brian L.
I am a health policy researcher with expertise in comparative effectiveness research, evidence based medicine, health technology assessment, cl...
Dana D.
Award-winning author and technical writer with expertise in content strategy, copywriting, and SEO-optimized storytelling. Experienced in craft...
Naresh S.
Regulatory Writing: Clinical Study Report, HA Responses, Literature reviews, Narrative writing, NDA-AR, IND-AR, CO and NCOs, Protocol, Investi...
Hayyan P.
I am a third-year MBBS student with a passion for medical writing and research. I specialize in creating high-quality health content, literatur...
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Laura F.
Results-driven commercial enablement leader with 20 years of healtcare-related experience in marketing, sales, training and product management....
Krishnakant S.
Regulatory Affairs and Toxicology Expertise: 1. Proficient in toxicological hazard assessment and human risk evaluation for product safety acro...
Majid T.
I have several years of experience as a scientific editor and peer reviewer for a wide range of high-impact journals and international conferen...
Dr. Muneeba A.
Need someone who can explain complex medical topics clearly and also write wellness content that actually connects with people? I do bot.... 👩⚕️ With a background in public health and pharmacy, I’ve written technical documents like...
Kristen D.
Innovative executive in clinical operations and regulatory affairs with successful experience in start-ups, hospital & CROs, private equity...
Dr. Raminder S.
Friendly and highly qualified Senior Scientist with 15+ years of international experience in molecular biology, genetics, tissue engineering, a...
Woodrow S.
I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...
Jayesh S.
I am a Biomedical Engineering researcher and freelance scientific writer with expertise in pharmacy, biomedical sciences, and healthcare resear...
Dr. Jan S.
🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...
VIVEK S.
I am a postgraduate in Medical Microbiology (M.Sc. Medical Microbiology) and currently pursuing a PhD part-time in the same field, with a stron...
Prafullakumar P.
I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...
Dr. Sevgi Ç.
14+ Years academic experience, expert in scientific writing, paraphrasing and biomedical documentation. Published author in SCI journals and b...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
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Dr. Anushikha D.
I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...
Dr. Ruchi A.
I'm a medical doctor (MBBS, MS Ophthalmology, Gold Medalist) and FICO (UK), with over 4 years' experience in tertiary care centers and ...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
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