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Woodrow S.
I am a Certified Quality Engineer and ISO 13485-trained Lead Auditor with a background in biomedical engineering and hands-on experience leadin...
Dr. Jan S.
🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...
Prafullakumar P.
I am medical devices regulatory affairs professional having expertise in following points - Author, Reviewer of Global Regulatory Technical Doc...
Consult top freelance Premarket Notification | 510(k) Submission experts for help with FDA submissions, technical documents, and more. Get help from top-rated 510k FDA submissions consultants with experience in medical devices, biotech and pharma.
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Looking for premarket notification 510k consulting services$550.00
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510k fda submissions consultants needed$450.00
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Need to outsource 510k submissions consultants$450.00
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What Is a 510(k) Submission?
A 510(k) submission enables companies, who want to market their product in the USA, prepare the necessary documents to demonstrate the safety, efficacy and effectiveness of the device intended to be marketed.
What Does a FDA 510(k) Submissions Consultant Do?
A 510(k) submissions consultant prepares premarket approval notifications, also known as a premarket notification 510(k). For devices requiring approval from the FDA before they can be marketed in the USA.
An FDA 510(k) submissions consultant enables,
- The device to be cleared by the FDA, declaring it to be legally marketed device
- The device to be found safe and effective under the appropriate regulation chapters of the FDA
- Help the business clear FDA quality system inspections anytime after the 510(k) clearance.
Qualifications for a FDA 510(k) Submissions Consultant
FDA 510(k) consultants typically have a degree in the related field of consultation, such as drug regulatory affairs, pharmaceutical technology etc. They hold a highly specialized knowledge of the USA market, and how the various regulatory chapters of the FDA operate.
In addition, 510(k) consultants also possess,
- Analytical and strategic skills to help them understand the precise steps to gain approval
- A deep domain knowledge of the regulatory requirements involved in 510(k) submissions
- Communication and negotiation skills
Benefits of Hiring Freelance 510(k) Submission Specialists
Whilst nigger companies typically have in-house 510(k) submissions experts, smaller organizations can benefit from turning to freelance consultants for their premarket approval consulting requirements.
Hiring freelance 510(k) submissions experts can prove to be,
- Time-effective, as they are available on-demand when the regulatory process is required
- Cost-effective, as they typically charge on a more affordable basis than full time employees
- Highly efficient, as organizations can hire the expert most suited to their requirements from across the globe.
Cost of Hiring 510(k) Submission Consultants
510(k) submission consultants on Kolabtree typically charge from $50/hour to $150/hour for various services, from regulatory document preparation to 510(k) premarket submissions.
Senior and highly qualified consultants, who might be required throughout the entire submission process might charge upwards of $250/hour for end to end consulting.
How to Post a Project to Hire 510(k) Submission Consultants
Whilst posting a project to hire 510(k) submission consultants, make sure you mention
- The precise scope and duration of the project
- The budget you’re willing to spend
- The exact skills you’re looking for (regulatory consulting, document writing etc)
These details will help you attract proposals from relevant experts on Kolabtree who match your niche requirements.
For further help, checkout this free Kolabtree Whitepaper on 510(k) submissions.
