Dr. Nare S.
My science qualification is Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...
Dr. Dilip B.
I am the holder of highly prestigious Tier 1 Exceptional Talent Visa and endorsed as such by the Royal Academy of Engineering in the fields of ...
Dr. Nael A.
Physician with over 12 years of clinical operations experience. Skilled in all aspects of clinical research support including trial management,...
Dr. Diksha V.
I am a doctorate in life sciences with an experience of over 9 years in the academic and corporate sector. I have managed projects focusing on...
An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR, ISO-10...
Food scientist with over 15 years progressive experience in food industry, with emphasis on R&D and Product development, both on the b...
Over 5 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...
Didy Yoga Lucky P.
I have experience in in vitro, in vivo, in silico study, analytical of plant extract, and isolation of metabolite. I also have written study to...
Biological engineer and cosmetic chemist, i have experience in cosmetic and biotechnology research and development. The cosmetics industry offe...
A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...
Regulatory Affairs Expertise in dietary and food supplements in the below markets with over 10 years experience. - Australia - Canada - US - E...
Dr. Vanshika S.
I am a published neuroscientist with collaborative research work appearing in journals like Oxford Academic's Cerebral Cortex and BMJ's...
Dr. Hafsa I.
Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...
Dr. Fabiola F.
Clinical Scientist | Digital Health Entrepreneur translating health innovation projects into clinically implemented realities.
Dr. Dipti S.
More than 16 years of extensive clinical research experience with expertise in following areas: Clinical Operations - Experienced in conductin...
PharmD with years of experience in the pharmaceutical/biotech space, from leading a multimillion-dollar pharma company to being directly involv...
- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...
Dr. Arinzechukwu U.
I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...
Dr. Ana Luiza C.
I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...
Dr. Shrinidh J.
I am an agile, performance-driven and critical problem solver scientist with a passion for scientific, pharmaceutical, medical devices, and str...
Hi Bindu, I am a hands-on cosmetic chemist with over 26 years of experience in developing wide range of skin care, hair care, make-up product...
Dr. Sonika V.
Experienced Medical Writer with a demonstrated history of working in the pharmaceutical industry and research organizations of international re...
Juan Manuel F.
Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 7+ years in clinical research Studies: I have a b...
Dr. Hrishikesh G.
Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...
Nanotechnology and Medical Device enthusiast with experience in New Product Development, Regulatory Affairs and Quality Management System. Work...
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.
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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.