Profile Summary
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. 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. 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. 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. Sreenivasarao B.
I have more than 24 years of experience in numerous positions of increasing responsibility internationally (New Zealand; Australia; Oman and In...
Dr. Amin Y.
Experienced Head Of Regulatory Affairs with a Demonstrated History of Working in the Biotechnology Industry. Skilled in Content Development, Tr...
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...
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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. 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. Evita A.
A clinical research scientific writer with clinical medical, CSR. and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and F...
Dr. Juliana D.
In recent years, I have assisted in various research projects in the fields of neuroscience, diabetes, stem cells, and developmental biology. I...
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. Operon S.
Operon Strategist is a medical device consulting companies which provides regulatory guidance to various manufacturers in the healthcare indust...
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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. Ioannis L.
Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...
During my PhD and postdoc research, I focused on facial morphology associated with orofacial clefting, as well as on the genetics of normal fac...
Dr. Maria Paula S.
I have a Bachelor degree in Food Science and Technology and PhD in Industrial Chemistry from the University of Buenos Aires. Highlights of my b...
Dr. Gabriela L.
I have a bachelor's degree in Pharmacy, a specialization in Regulatory Affairs, and a master's degree in Pharmacology from UFMG, where ...
Dr. Ewa M.
I am an economist specialising in competition and regulation issues. I obtained a PhD in industrial organisation from Erasmus University in Rot...
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
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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Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.
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Our T&C include a default confidentiality clause that protects your IP. Sign NDAs 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 clause. You can also sign NDAs and custom agreements with freelancers for additional protection.
Post your project and receive quotes from relevant freelancers. You can also search for specific freelancers by expertise and invite them to your project. Discuss your project details with each freelancer before picking the one best expert.
We assure you of a 100% satisfaction guarantee, which means you only pay when you’re 100% satisfied with the work delivered. If you aren’t happy, we will refund 100% of your money.
You can choose to pay either a fixed or an hourly fee based on your scope of work. If you’re not sure how much your project costs, you can discuss with freelancers before arriving at a mutually agreed fee.
Kolabtree's terms and conditions prohibit freelancers from claiming ownership of intellectual property, and as a client, you are able to reinforce the message with additional communication, agreements or contracts.
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Pay a fixed or hourly fee. We hold your funds securely until you’re ready to pay.
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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.
