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Dr. Souad M.
I am a hard working and dedicated Clinical Researcher with 20 years of experience in clinical research in the fields of Neurology, Cancer, Card...
Dr. VANOJAN M.
I am a medical doctor and a medical writer and editor for the past 8+ years. I have worked with many researchers, surgeons, dermatologists, nep...
Dr. Timos N.
Highly motivated executive with a broad experience in clinical research, academia and industry fields. Successfully managed clinical trials pha...
Dr. ANUSHA C.
I am a doctor with a bachelor's degree in medicine (equivalent to an MD in the USA) and a specialization in preventive medicine. My experti...
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Dr. Muhammad Hashim Ghouri, PT embodies the epitome of dedication and excellence as a preeminent Pulmonary and ICU Rehabilitation Specialist. D...
Dr. Dr akshay MD Senior medical writer A.
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Krishna K.
Clinical Project Management and Medical Writing professional with 11+ years of experience in bio study activities including project planning, m...
Vasil I.
Local literature review, Legislation monitoring, Handling safety information, Participating in project specific audit.
Summer A.
I am a motivated multitasker with 15 years of clinical and 25 years of preclinical peer-review publication experience. I have served as a revie...
Dr. Martijn S.
I have 25+ years experience as an academic health researcher, including 14 years as full Professor. My expertise is in the epidemiology, biomec...
Tarushi P.
Centre for cruelty free testing is a DST-FIST centre by department of science & Technology, Govt. Of india. We are amongst few labs t...
I am working in a medical institute for 9+ years as faculty orthodontist. Currently, I am Associate Professor with responsibility including aca...
Dr. Jennifer S.
Medical and science writer with experience in regulatory and academic documents. I have a background in health research and teaching from McMas...
- More than 10 years of experience as a biostatistician - Have worked in many fields (onco-hematology, transplantation, biomarkers, immunology)...
Dr. Indrabahadur S.
Hello everybody, I am Senior Scientist at German Cancer Research Center (DKFZ), Heidelberg, Germany and editorial board member of SM Journa...
David C.
Hello! Thank you for considering me for your next project. During the course of my career I have learned that the most exciting part of the sc...
I have been working in the registration of investigational medical devices and pharmaceuticals since 2005. During that time, I have worked with...
Anjali S.
Performance-driven professional with total 2 decades of rich & extensive experience in Clinical Research & Development, Pharmac...
GURUDATH G.
Entrepreneur, Design Thinking Master Practitioner & Human-centred Innovation enabler Clinical Research Leader with 8+ years of Project,...
A highly analytical and creative epidemiologist with experience managing biological data as well as large cohort data using statistical program...
Dr. Amro A.
I am a scientist working in an immuno-oncology biotech and I also have a medical writing consultancy (Amro Biopharma Consulting, Ltd). I have ...
Joshita M.
A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...
Alifiya T.
I am a research scientist and medical writer trained in clinical trials research (MPH, Rutgers University, USA). I have experience working acro...
Dr. Sonya D.
We are a consultancy staffed with several scientists and business experts. ...Our typical scientist has an impressive publication record and PhD + approximately ten years of experience...
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)
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.
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.