Profile Summary
Anand K.
Regulatory Affairs Services like ANDA, ANDS, Pre-IND, Control Correspondence, DMF, APIMF, CEP, and Dossier (Rest of World).
Dana D.
Award-winning author and technical writer with expertise in content strategy, copywriting, and SEO-optimized storytelling. Experienced in craft...
Roopsandeep B.
Determined and result-oriented Academician, Researcher, Professional and Entrepreneur, possessing excellent analytical and communication skills...
Dana C.
Scientific editor specializing in publications on various topics in medical sciences, such as diabetes mellitus, nutrition, cancer, maxillofaci...
Hebatallah E.
sharing the opportunity to collaborate on your regulatory submission and medical communication project. As a highly rated professional medical ...
Dr. Muhammad Akbar R.
Dedicated Public Health Researcher and Healthcare Professional with extensive experience in epidemiology, maternal and child health, and optome...
Dr. Raj V.
Experienced scientific and regulatory affairs professional, trained in drug discovery and development working with novel small molecule drugs, ...
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...
Shaheen Fathima A.
I am a Regulatory Affairs and Clinical Research professional with expertise spanning drug development, compliance strategy, and scientific docu...
Alex H.
AI-driven biotech and translational science consultant with 25+ years of experience across discovery, preclinical, and IP strategy. I help biot...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Dr. Robin A.
I deliver audit-grade, regulator-defensible, visually flawless governance and scientific documents that survive FDA, EMA, and courtroom scrutin...
Idalina M.
PhD-level scientific and medical writer with 15+ years of experience delivering publication-ready manuscripts, regulatory documents, and high-i...
Spencer D.
I am a seasoned academic and consultant with over 15 years of experience in business education, policy research, and economic strategy. As a...former Assistant Professor, I taught undergraduate and graduate courses in finance, economics, and public...
Nathan O.
CMC leader at Cayuga Biotech, specializing in pre-clinical and early clinical manufacturing, scale-up, and regulatory writing.
Dr. Joseph B.
Dr Joseph B. Babigumira is a physician-economist whose two-decade career blends frontline clinical insight with advanced economic evaluation, h...
Dr. Harriet K.
Regulatory writing and submissions • Regulatory Intelligence and Strategy Development • Toxicology Study Monitoring • Due Diligence and Gap Ana...
Dr. Jan S.
🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Nikolaos D.
I am an Analytical Development Scientist and Biochemist (PhD in Drug Delivery & Microbiology) with over a decade of experience in biologics...
Dr. Robbie C.
AI/ML Engineer and Data Scientist with a decade of experience driving digital health innovation from startup inception to large-scale data solu...
Sharoon A.
I am a PhD candidate in Biochemistry and Molecular Biology at Mayo Clinic, specializing in serine proteases and translational oncology. My rese...
Dr. Anurag G.
As a clinical research professional with advanced Pharm.D. training, I bridge the critical gap...between complex scientific data and the clear, persuasive content required for regulatory approval, publication...
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