Profile Summary
Dr. Amin H.
I never planned to spend my career listening to the heart, but that’s where science led me. For the past decade, I’ve been obsessed with one q...
Tina O.
●Author of 20+ substantially equivalent FDA 510(k) premarket notifications; De Novo and IDE applications, and ROW submissions in over 110 count...
Dr. Lorena P.
Lorena is Bioengineering Technical Leader | Innovation & Process Excellence Expert Accomplished PhD Chemical Engineer with over 14 years...
Silvija B.
I am a regulatory and technical documentation specialist with 20 years of experience working in a highly regulated ISO 17025 laboratory serving...
Dr. Sotirios B.
Experienced scientific editor with a passion for helping fellow researchers share their innovative work with the world. With >6 years of exp...
Maika L.
I am a Data Scientist with a background in Biology and 7 years of experience in the corporate healthcare sector. I specialize in bridging the g...
Eddie W.
I'm excited to help businesses reach market approval on their new or existing medical devices and IVDs. I have experience working with both...
Raksha R.
I am a biotech strategy consultant specializing in competitive intelligence, regulatory pathways, and market access strategy for rare disease t...
Bruce T.
I have a Bachelor's in Biomedical Engineering from Toronto Metropolitan University (formerly Ryerson) and a Master's of Biomedical Engi...
Andrew D.
Senior Combination Product and Design Assurance Engineer with extensive experience delivering drug–device combination products, primary packagi...
Kimberly K.
Clinical research and medical writing consultant with over 15 years’ experience supporting medical device and biologics companies across their ...
Soutik D.
About Me I am a Regulatory Affairs professional with hands-on internship experience in the pharmaceutical sector, specializing in drug dossier ...
Rajesh K.
Take up projects in all areas of Quality and Regulatory of MedTech, Automotive and High Tech
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Jamila A.
I help MedTech companies bring regulated products to market — from early development through regulatory submission — with a particular focus on...
José Daniel C.
Biomedical Engineer, Microbiologist, and Master of Public Health (MPH) with over 5 yea...experience in the global medical device industry and healthcare public affairs....
Dr. Adam S.
Former university professor & PhD-qualified academic consultant with 12 years of experience delivering publication-ready dissertations, the...
Jarrell M.
I am a medical device consultant with 25 years of experience helping companies bring products to market. I combine strong expertise in regulato...
Dr. Elma H.
Elma Hrustemović, DVM, Academic Specialist in Clinical Microbiology and PhD Researcher, is a dedicated scientist at the University of Sarajevo,...
Andrei L.
I bridge the gap between clinical requirements and advanced AI architecture. With a strong background in Healthcare & Medicine and deep tec...
Dr. Florence L.
Medical Device and In-Vitro Diagnostics Regulatory Affairs and Quality Assurance (QARA) professional with 6+ years’ experience supporting medic...
Dr. Seval K.
Quality Assurance , Validation Planning and Reporting , Medical Device Clinical Study Design and Reporting by CER PSUR and else. , FDA Register...
Dr. Muhammad W.
ASCPi-Certified (USA) & SCFHS-Licensed (KSA) Medical Laboratory Scientist with over five years of high-impact clinical and research experie...
Alicja Z.
I help medical-device manufacturers, importers and authorised representatives with EUDAMED actor registration (SRN) and device registration und...
Ashley K.
Regulatory Affairs and Quality Assurance specialist with nearly three years of hands-on experience supporting medical device and IVD manufactur...
Kolabtree is the leading online marketplace for ISO 14971 experts. Post your project, get bids, and hire qualified experts quickly and easily.
We take several measures to help you work with full confidence and peace of mind.
Keep your project private
Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.
NDAs and IP protection
Our T&C include a default confidentiality clause that protects your IP and NDA for added protection before disclosing project details.
Kolabtree ensures the safety and security of your payments, personal information and project details. Kolabtree’s T&C include a default confidentiality and NDA clause.
You will receive detailed proposals directly from Kolabtree. These proposals will include a comprehensive Statement of Work (SOW), project fees, milestones and deadlines.
You can choose to pay either a fixed or an hourly fee based on your scope of work. Pre-pay for the next milestone. You have to approve the deliverables only if the quality meets your expectations. If you aren't happy, we'll refund your money.
Kolabtree will share multiple quotations for your project. You have the freedom to accept the quote that aligns with your project requirement and budget. You can get in touch with us if you want to discuss the fee.
Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
Contact experts directly
Speak directly with freelancers and explain your requirements.
100% satisfaction guaranteed
You have to approve the deliverables only if quality meets your expectations. If you aren't happy, we'll refund your money.
Project Management
Keep track of files and conversations in the user-friendly Workspace.
Flexible, secure payments
You can choose to pay either a fixed or an hourly fee based on your requirement.
Post your Project (Free)
Your project details are safe, secure and visible only to logged-in users.
Get Quotes & Choose Experts
Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.
Collaborate
Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.
Job Done!
Approve the deliverables once you're satisfied with the job done.