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Laura F.
Results-driven commercial enablement leader with 20 years of healtcare-related experience in marketing, sales, training and product management....
Majid T.
I have several years of experience as a scientific editor and peer reviewer for a wide range of high-impact journals and international conferen...
Kristen D.
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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...
Dr. Sevgi Ç.
14+ Years academic experience, expert in scientific writing, paraphrasing and biomedical documentation. Published author in SCI journals and b...
ALOKEPARNA C.
I help medical device startups, diagnostic innovators, and digital health companies build robust and compliant documentation aligned with ISO 1...
Jarrell M.
I am a medical device professional with 25+ years of experience in R&D product development, risk management, and regulatory compliance. Thr...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
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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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.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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You can choose to pay either a fixed or an hourly fee based on your requirement.
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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.