Profile Summary
Dr. Laila A.
I have been working in medical research since 2009, I had the opportunity to work in the Pharmaceutical and Medical Research center. I worked a...
Dr. Hatem D.
Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox- PRP -etc) , with 15+ years of expe...
Dr. Melisa S.
Experienced researcher with scientific knowledge and expertise in several therapeutic areas, including: metabolic disorders, ophthalmology, gen...
Dr. Ethiene C.
I am a Biomedical Scientist with a multidisciplinary background. I hold a Master's and a Ph.D. in Pharmacology and have worked as a researc...
Dr. Precious O.
I am experienced in
Dr. Suriya S.
✔Prodigy for bringing the change in the Concept of Cord Blood Banking Industry from 2016 ( Preservation and Utilization of Cord Blood units th...
Dr. Srivani V.
Expert in cell-based therapies, chemistry, bio-nano fusion science, tissue engineering, organ models, cancer/immunology/CNS pre-clinical and tr...
Dr. Juveria U.
I am PhD research scholar with three years of research experience in the field of pharmacology and specialised in clinical research. i have des...
Dr. Amare Worku K.
Doctor of Medical Sciences, with more than 20 years of laboratory diagnostics, quality assurance, leadership, and research experiences in healt...
Dr. Irina P.
I have a robust academic foundation in health and life sciences coupled with 7 years of experience as a Research Fellow in the field of nanotec...
Dr. David T.
Corporate communications, business writing, graphic design. Extensive research, writing and editing experience, computer-aided design and layou...
Dr. Scott F.
Biomedical professional with a multifaceted background in research in an academic setting, 5-years at the FDA in the Office of Orphan Products ...
Dr. Juliana D.
Team manager for RA and Quality, Regulatory Affairs: CFDA Registration experiences in Medical device field,(imported Class 3 MD includes Defibr...
Dr. Sreenivasarao B.
I have more than 24 years of experience in numerous positions of increasing responsibility internationally (New Zealand; Australia; Oman and In...
Dr. Leticia M.
I am a pharmacist with a PhD in chemical and bioprocess engineering, working as a bioprocess scientist. I have experience with cell culture, up...
Dr. Amin Y.
Experienced Head Of Regulatory Affairs with a Demonstrated History of Working in the Biotechnology Industry. Skilled in Content Development, Tr...
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Dr. Fady R.
PharmD with years of experience in the pharmaceutical/biotech space, from leading a multimillion-dollar pharma company to being directly involv...
Dr. Michelle M.
✰ Open to Work ✰ Available for Short & Long Term Engagements ✰ ✰ Available for due diligence, consulting, advisory, leadership and boa...
Dr. SREEDHAR T.
Post Graduate Medical Doctor, MBA in Healthcare and PGdiploma Herbal drug Technology with 15+ years of experience in Clinical Research,Herbal D...
Dr. Ângela P.
I am a Pharmacist with ten years of experience with clinical research, pharmaceutical patient care services, pharmacovigilance and regulatory a...
Dr. Paula P.
- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...
Dr. Ioannis L.
Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...
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Dr. Rita B.
A health economist with 12+ years of expertise in academia and industry worldwide. Business strategist. Expert in economic modelling and predic...
Dr. Eric L.
With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...
Work with freelance regulatory affairs consultants for product development support. Medical devices, pharmaceuticals, biologics, biosimilars, and more. Get help with FDA submissions, regulatory affairs consulting services, MDR compliance, and more.
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 safety and security of your payments and personal information and project details. Kolabtree’s T&C includes 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 arn’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 in case 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 arn’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.
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Hiring for regulatory affairs specialists$550.00
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Regulatory affairs expert needed$440.00
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Looking for regulatory affairs consulting services$600.00
Post your Project (Free)
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Get Quotes & Choose Experts
Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.
Collaborate
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Job Done!
Approve the deliverables once you're satisfied with the job done.
What is a Regulatory Affairs Consultant?
A regulatory affairs consultant helps companies obtain the necessary accreditation and permissions involved in the manufacture and distribution of drugs, medical devices and related products.
What Does a Freelance Regulatory Affairs Consultant Do?
A regulatory affairs specialist uses scientific research, knowledge and analysis to ensure the safety and efficacy of various products before they hit the market. This includes medical devices, healthcare products, pharmaceuticals etc.
Through this product check, a regulatory affairs specialist ensures that the product meets the various regulations mandated by local and international federations, including safety and compliance requirements.
Qualifications for a Regulatory Affairs Specialist
Regulatory affairs consultants typically hold a bachelors or masters degree in the niche field they operate in, such as biochemistry or pharmaceuticals. They also have a thorough understanding of the various regulations and compliance requirements involved in the product they’re being consulted for.
In addition, regulatory affairs consulting service experts also have,
- A good understanding and anticipation of evolving regulatory rules that might impact the business and product
- Ability to document and explain the rules, protocols and procedures to all the employees and stakeholders.
- Analytical skills and ability to maintain audits, as well as marketing and legal documentation, for the purposes of assessing compliance.
Benefits of Hiring Freelance Regulatory Affairs Specialists
Regulatory affairs specialists typically consult on-demand, as and when the business needs review and compliance for new products. This provides great business value for the company, as they can turn to freelance regulatory consultants for,
Recommending a course of action to help the company achieve compliance and eventually go to market
Help the company prepare the necessary paperwork and ensure approval from the necessary government bodies.
This also gives the company the opportunity to hire cost-effective regulatory affairs consultants who can be hired as and when the demand arises. Freelance consultants typically can be hired from anywhere in the world, enabling the companies to pick and choose the best expert regardless of location.
Cost of Hiring a Regulatory Affairs Expert
The cost involved in hiring a regulatory affairs expert varies according to the duration of the project, and the exact niche of consulting required.
On Kolabtree, you can hire a regulatory affairs consultant from $40/hour up to $150/hour, whilst senior regulatory affairs specialists charge around $225-300/hour.
How to Post a Project to Hire Freelance Regulatory Affairs Consultants
Before posting a project, take into account the following,
- How long you need to hire a regulatory expert for
- The exact niche and expertise you need
- The budget you’re willing to spend
Now, post a project on Kolabtree based on these criteria, which will help you attract relevant proposals from your project. Then, you can browse through the various regulatory affairs consulting services experts, review their educational and work credentials, and find one that best suits your requirements.
