Featured EU MDR Consultants
Our freelancers have helped medical device manufacturers of all sizes achieve regulatory compliance. Speak to an expert directly for help with MDR gap assessment, CE transition, EU MDR compliance checklists, MEDDEV 2.7/1 rev 4, clinical evaluation reports, technical documentation, and more.
Experienced CER Writer
Has worked on CERs for Johnson & Johnson,
Abbot, and more
LocationUnited States
Rate USD 85 per hour
Experienced CER Medical Writer
Has worked on CERs for Medtronic,
Abbot, and more
LocationUnited States
Rate USD 75 per hour
Medical Device CER & Regulatory Writer
Evidence Evaluation Specialist for Smith & Nephew
LocationUnited States
Rate USD 60 per hour
CER Medical Writer
Clinical Research Scientific Writer
LocationUnited States
Rate USD 110 per hour
Why Kolabtree
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Our T&C include a confidentiality clause and IP protection but you can sign NDAs with experts as an additional safeguard. Make your project visible only to specific freelancers.
Risk-free
Speak directly with freelancers to ensure that they have the right skills required for your project. Use milestones and timesheets to easily track progress.
100% Satisfaction guarantee
Release funds to the freelancer only if you’re 100% happy with the work done. Pay by the hour or pay a fixed fee.
Whether you need a one-hour consultation call or a long-term project, Kolabtree’s experts are ready to help.
EU MDR Medical Device Compliance: Solutions to the resource crunch
The EU MDR is one of the biggest changes to medical device regulations in the last 20 years. Read how medical device manufacturers are affected and what can be done to overcome challenges. This white paper covers:
- Barriers to EU MDR compliance
- Solutions to overcoming barriers
- The role of on-demand experts and consultants
Download the Free White Paper
Please enter your company email address below to receive the white paper.
Contact trusted EU MDR consultants, on demand.
Improve your chances of getting a CE mark quickly.
- Consult experts who can help you prepare a robust and comprehensive compliance plan
- Get help from experts to navigate grey areas and understand MDR compliance requirements specific to your device class and therapeutic area
- Hire freelance CER writers with 3+ years of experience
- Get help with specific sections of the clinical evaluation report such as literature reviews, clinical data analysis and systematic reviews
- Outsource technical documentation (risk-benefit analyses, instruction manuals, safety assessment) to qualified regulatory writers
How It Works
1
Post a project (free)
Describe your project, choose your budget, and select the service you need.
2
Choose the best expert
Get bids from relevant experts. Interact freely with them before making a hire.
3
Collaborate
Share files, make audio/video calls and collaborate with your chosen expert.
4
Complete project
Verify the project is complete to your satisfaction before paying the expert.
What our customers say
"Indispensable part of my team"
Kolabtree was the single best professional decision I have made in quite a while. I was faced with completing a complex project in a short time period and was looking for a reliable consultant. I contracted with a brilliant biostatistician and his team who not only completed my project before my deadline but also enhanced my analysis with their insights. Kolabtree is now an indispensable part of my business development and project implementation team.
Robert Goldberg
Co-founder of The Center for Medicine in the Public Interest, New York, USA
"Exceptional quality of work"
We used Kolabtree as a fast and easy way to get in touch with medical and science experts for various consulting projects. The quality of experts available was excellent and we have typically found selection, bidding and hiring to be effortless. All of the consulting projects that we placed through the platform were successful and the quality of work was exceptional. We will continue to use Kolabtree for locating and hiring technical experts for consulting projects.
Alex Lucio
Executive Vice President, 3B Medical, Inc. Florida, USA
Success Stories
No matter what the size of your business, Kolabtree’s PhD-qualified specialists are ready to help. Save time and energy by consulting our medtech experts.
- Secondary Research
- Medical Device
Help with medical device innovation
The founder of a US-based medical device company hired a scientific writer to provide supporting research for the launch of a new product.
Read Story
CostUSD 2750
Time Taken20 Days
- Scientific Consulting
- Medical Device
Develop a medical device
An Australian medical device innovation company hired a Mexico-based nanotechnology expert to develop electrodes that could destroy living tissue.
Read Story
CostUSD 2000
Time Taken1 Month
- Experiment Design
- Healthcare
Design a clinical trial
A California-based breast cancer surgeon hired an India-based biostatistician to design a clinical trial.
Read Story
CostUSD 1575
Time Taken2 Weeks
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Skills related to EU MDR consulting
