Profile Summary
Anil C.
Working towards catalyzing the Strategic Development of the Clients in the regulatory, quality assurance, manufacturing process development, pr...
Michael L.
I am an accomplished professional with a PhD in Optoelectronics and Laser Systems, along with an Executive Certificate in Innovation Management...
William T.
Experienced Technical Writer and Laboratory Scientist adept at managing and executing multifaceted projects within stringent timelines. Profici...
Veer P.
A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...
Aida S.
I’m a PhD-trained medical writer and scientific strategist with 12+ years of experience spanning academic research, peer-reviewed publishing, i...
Ayoub B.
I am a trilingual Biomedical Engineer (French/English/Arabic) with dual academic training from UTC Compiègne (France) and ENSAM Rabat (Mor...
Dr. Somnath Swami V.
Researcher with expertise in solubility enhancement and formulation development of pharmaceutical compounds, focusing on the use of mesoporous ...
Devin M.
I help medtech companies design, assess, and improve quality systems to ensure regulatory compliance, streamline development, and prepare for a...
Dr. Ark K.
I am a PhD-qualified molecular biologist with over 20 peer-reviewed publications and scientific books. For the past 8 years, I’ve worked in the...
Dr. Umadevi R.
A Seasoned Medical Writer and Regulatory Affairs professional with a Ph.D. and extensive expertise in authoring high-impact clinical and regula...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Sohanur R.
Pharmaceutical quality and compliance specialist with over 15 years of experience in sterile manufacturing environments. Holds a Master’s degre...
Deepa K.
I’m a passionate **Biochemistry postgraduate** with over **10 years of hands-on experience in Research & Development**, driven by a deep cu...
Dr. Diana K.
I’m a medical doctor (OB/GYN), bioinformatics & data science graduate, and experienced medical writer with 4+ years in clinical trial suppo...
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...
Dr. Patricia D.
I am a Pharmacist with a PhD in Sciences Applied to Health Products (UFF) and a Master’s degree in Pharmaceutical Sciences (UFRJ), combining ov...
Karissa T.
I’m a seasoned Regulatory Affairs Consultant with over 17 years of experience supporting medical device and IVD companies in achieving global c...
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 ...
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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...
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Edwin M.
As a content writer, I craft compelling content that not only engages readers but also drives traffic. With a keen eye for detail and a deep un...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
Dr. Ziaullah Z.
Bridging the gap between complex chemical problem-solving and strategic regulatory navigation, I contribute to the development of innovative ph...
Dr. Vinay V.
I am a Research Scientist specializing in Biosensors and Translational Diagnostics, with over ten years of experience across academia, clinical...
Kolabtree is the leading online marketplace for EU In vitro Diagnostic Regulation (IVDR) Compliance experts. Post your project, get bids, and hire qualified experts quickly and easily.
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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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