Profile Summary
Passionate Food Scientist and Chef Developer with an MSc in Food Innovation and Product Design, BSc in Food Science and Technology (Valedictori...
I provide services in each stage of cosmetic product life cycle. I am having 5+ years of experience in Cosmetic Product Development in India an...
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
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Bradley P.
Dedicated to helping mid to large-scale companies drive greater value and ROI through innovation process management and partnerships. My expert...
I am having experience in Medical writing, Regulatory affairs, Pharmacovigliance, i am able to do dossiers work, Licence work.
An experienced Regulatory Affairs professional with significant industry know-how across food supplements/nutraceuticals/foods products. I am a...
Nanotechnology and Medical Device enthusiast with experience in New Product Development, Regulatory Affairs and Quality Management System. Work...
EXPERTISE 18+ years of experience working with companies across Asia, Australia and Canada Quality Assurance, Compliance & GMP Coor...
Juan M. C.
Juan M. Campos is a Medical Device professional with + 33 years of continued industry experience. His main areas of expertise include Quality A...
Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...
Pharmaceutical Regulatory Affairs professional with more than 10+ years in industry experience in Formulations.
Medical device professional with strong background in single use disposables, reusable medical devices(Class I, Class II and Class III) . Broad...
I have a Master's degree in pharmacology with about 7 years of experience in both CMC and the Clinical domains of regulatory affairs. I am ...
Excellent team spirit, own initiative, love teamwork, responsibility and capacity to manage conflicts, ability to adapt to different contexts,...
Khushbu P.
I am Khushbu Pitroda, completed masters in pharmacy (Pharmacology) in 2015, Bachelor of pharmacy in 2013 and Diploma in pharmacy in 2010 from G...
Tasmiatul K.
1. Registered and Licensed Pharmacist (RPh) in Bangladesh (Reg. No- A 4845) 2. Experienced Professional equipped with skills in the field of Re...
Mr. Khalil’s professional career spans over thirty (30) years of executive and entrepreneurial leadership in pharmaceutical, medical devices, n...
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Deliver wide range of regulatory affairs services, including CTD audit dossier, proof reading, translations, variations, document compilation n...
Coordinated multiple number of regulatory and pharmacovigilance projects such as finalizing regulatory strategy roadmap, technical review of co...
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
A proactive and result-oriented medical device professional with over 25 years of experience in QMS Systems and Regulatory Affairs compliance. ...
Motivated, self-driven entrepreneur, consultant to regulatory affairs and QC/writing departments within the medical, biotech and pharmaceutica...
I am performing as a clinical research consultant since Dec 2017. I had more than a decade of experience in all the domains of clinical researc...
Vandana C.
Experienced leader with a demonstrated history of global project management in the CRO with over 9 yrs of successful experience in Regulatory 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. 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 only once work is delivered and you’re happy with it.
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No minimum commitment or contract required.
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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.
