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. 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...
Dr. Amin H.
I’m a PhD-level Medical Writer and Biomedical Engineer with over 10 years of experience in clinical research, scientific writing, and regulator...
Lakshmi Rohini T.
Postgraduate in Microbiology from the Central University of Tamil Nadu with an advanced diploma in Clinical Research. I have hands-on research ...
Dr. Fernando T.
🎓 PhD-level Pharmacologist with over 6 years of experience in preclinical research, pharmacology, and biomedical sciences with scientif...
Dr. Shifa J.
Regulatory Affairs and Scientific Research professional with 6+ years of combined experience in biotech, academia, and government. Skilled in r...
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...
Antonio L.
I hold a Doctor of Medicine degree and have over 10 years of professional experience in medical writing for various healthcare, scientific, and...
Dr. Oleksiy V.
Experienced clinical research leader with 20 years of experience in clinical trials, including 18 years in Regulatory and Start-Up (RSU). Demon...
Dr. Annunziata C.
I have worked on a wide variety of fields and on a plethora of pathological and physiological contexts, from basic to translation and then pre-...
Dr. Krishnaa U.
I am a Clinical Pharmacologist and Clinical Research Professional with 13+ years of global experience across pharmaceutical industry, CRO opera...
Dr. Allan A.
Dr. Allan Ayella is Founder, and Chief Scientific Officer for ADEK BioPharma LLC, a consulting firm in chemistry/biochemistry research, food te...
Dr. Guillermo A B.
As a Physician with an MBA in Healthcare Administration, I bring a unique blend of clinical expertise, research operations, and academic writin...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Anurag G.
As a Doctor of Pharmacy (Pharm.D.) graduate, I possess deep clinical and research expertise from hospital, academic, and community healthcare s...
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.
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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.
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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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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
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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.