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Kolabtree connects organizations of all sizes with on-demand experts from all across the globe. Medical device organizations use Kolabtree to hire the best talent in medtech research, communication and product development. Our vetted subject matter experts provide insights that help medical device innovators accelerate growth and reduce time to market.
SECTOR: Regulation
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| We manually screen each profile and can handpick the best freelancers for your project. |
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| We offer a 100% satisfaction guarantee that assures you of a safe and risk-free experience. |
Kolabtree connects organizations of all sizes with on-demand experts from all across the globe. Medical device organizations use Kolabtree to hire the best talent in medtech research, communication and product development. Our vetted subject matter experts provide insights that help medical device innovators accelerate growth and reduce time to market.
Safe, secure and risk-free
Kolabtree is a trusted partner for medtech businesses worldwide. We offer an unparalleled quality of experts, confidentiality assurance and a 100% satisfaction guarantee. Main benefits include:
Fast, flexible solutions
Kolabtree’s medical device consultants are specialists in all medical device classes and therapeutic areas. Our vetted subject matter experts include:
Regulatory Writers
Get end-to-end support for developing and submitting 510(k) and PMA applications to the FDA. Our experienced Clinical Evaluation Report writers can help with EU MDR requirements.
Medical Content Writers
Get help from qualified freelance medical writers to develop authoritative, SEO-friendly content for blogs, white papers, brochures, and more.
VIEW FREELANCE MEDICAL WRITERS
Medical device development consultants
Our product design experts can help you develop a market-ready product while ensuring regulatory compliance.
Freelance Medical Statisticians
Get help with complex data analysis, statistical methodologies and study design optimization so that you get the best outcomes from your research.
Clinical Trials Consultants
Work with our freelance biostatisticians to design robust research studies and interpret the results accurately.
Hiring experts on demand is perfect for SMBs with one-off requirements and limited budgets. On Kolabtree, you have complete flexibility while hiring: you can personally view, invite and select freelancers to work with. Medical device businesses have cut costs of up to 40% by working with Kolabtree’s on-demand experts.
Kolabtree Limited
Devonshire House,
60 Goswell Road,
England,
London,
EC1M 7AD.
Email address: contact@kolabtree.com
Hire CER and Meddev 2.7/1 rev 4 experts for compliance with EU MDR. Work with experts for literature search, gap analysis, EU MDR 2017/745 compliance reports.
Consult top freelance clinical evaluation report writers with 5+ years of experience having expertise in clinical evaluation documents writing, clinical study reports, clinical evaluation statistics and more.
Consult top 510(k) submission experts for help with FDA submissions, technical documents, and more. Get help from top-rated regulatory writers with experience in medical devices, biotech and pharma.
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.
Consult top freelance regulatory medical writers with expertise in clinical regulatory writing, regulatory writing services, and more. Get end-to-end support for developing and submitting applications for approvals, whether they are FDA applications or NIH SBIR grants. Get all the technical documentation you need to get a CE mark.
Get expert help with SEO friendly medical content writing, editing, fact-checking and more. Services offered - article writing, expert review, CME writing, medical communications.
Take your medical device to market easily with the help of our global pool of experts. Get help with all the technical documentation you need to get a CE mark. Qualified and experienced freelancers ready to help you with various services like: IVDR, ISO 13485, Medical device literature reviews, IDE, Diagnostic imaging, Medical device development, ISO 14971 and more.
Consult qualified and experienced freelance medical writers to communicate your product features and benefits to your target audience. Get help to write content on various topics like pacemaker, ultrasound, medical implants, wearables, catheter, ECG, collagen and more.
Applying for FDA approval can be nerve-wracking but consulting with experts who have a detailed knowledge of FDA procedures can streamline the process. Hire top FDA submission experts for help with regulatory writing to increase your chances of approval.
In Part 1 of our series covering the major medtech, biotech and healthcare players in the world, we take a look at the medtech companies in Europe driving pioneering change in the industry.
Medical device companies have several crucial steps in their journey from conception to research to product development, and freelancers play a key role in all several aspects along the way. Developed by Kolabtree, this FREE white paper gives you a comprehensive view of everything you need to know to hire the best talent for your medical device company.
To help science and medical publishers produce high-quality content, meet tight deadlines and reduce pressure on in-house writers, Kolabtree has released How to outsource content creation: The ultimate guide for science publishers. The whitepaper explores the benefits of outsourcing content writing, challenges publishers face when putting together content and the different types of content that freelancers can help produce. The white paper can be downloaded for free here.
Expert network Kolabtree has announced the release of a new free resource for medical device manufacturers: The essential technical file checklist. Developed by regulatory experts, the checklist is aimed at medical device companies who want to place a device in the EU market and need to comply with MDR guidelines. It’s available to download for free here.
The medical device outsourcing market is expected to grow at a CAGR of 11.2% over the next few years, reaching USD 227.1 billion in 2028.
Ashmita Das, Kolabtree co-founder, discusses the challenges in COVID-19 vaccine manufacturing and the future of biomedicine with biotech entrepreneur Jacob Glanville.
LONDON, May 17th, 2021: Kolabtree.com, the freelance platform for scientists, has announced that it now has over 20,000 registered freelancers on board. This new milestone cements the company’s position as the world’s go-to platform for scientific expertise.
As the popularity of remote working rises amidst the pandemic, businesses are turning to freelance platforms like Kolabtree to hire scientific experts on-demand.
To help small and medium medical device manufacturers benefit from access to the skills of freelance scientific experts, Kolabtree has released The complete guide to freelancers in MedTech. The whitepaper explores the benefits of collaborating with experts at every stage of the medical device lifecycle and explains the factors to consider when working with a freelancer. The whitepaper can be downloaded for free on the Kolabtree website here.
The Challenge: A Sydney-based organization providing innovation support for medical device manufacturers was looking to create a new product. They were scrutinizing for an expert who could help them formulate the product. How Kolabtree Helped:
The Challenge: Jon P. Mendelson, Chief Operating Officer at Chemo Mouthpiece, a US-based medtech company, had developed an oral cryotherapy device to help cancer patients manage the side-effects of chemotherapy and radiation therapy. He was looking to launch his product in the market. However, he needed supporting documentation for his product, including a compilation of all relevant research articles, clinical trials, and a summary of outcomes.
The Challenge: Alandra Medical, a Mexico-based medical company had just finished a pre-clinical study which tested the safety and efficacy of their medical device. They were looking for a statistician to verify if their results were accurate and help them develop a report for publication.
