Spotlight: Kolabtree’s Regulatory Medical Writer Dr. Nare Simonyan
Kolabtree’s freelance scientist and regulatory medical writer Dr. Nare Simonyan sat down with us for…
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FDA 510k Submissions Guide: Free Kolabtree Whitepaper
510k submissions are an integral part of entering the USA medical device market, and help…
How Healthcare Writers Can Help Your Business
Healthcare writers possess expertise across medicine and life sciences. Their creativity and flair for narration…
The Benefits of Outsourcing in Continuing Medical Education (CME)
Medical Education, or Continuing Medical Education (CME) refers to the ongoing learning and education process…
The Definitive Guide to Hiring Curriculum Writers
Independent curriculum writers and specialists can work on flexible schedules, and provide on-demand expertise, to…
Risk Management in Medical Devices: Evaluation, Mitigation & Management
Ensuring risk management in Medical device is a continuous process, and medical device manufacturers have a…
Hire a Data Scientist – The Complete Guide
Data science is one of the most frequently hired jobs right now, with the need…
Hire a Grant Writer – The Complete Guide
Looking to hire a grant writer? Here’s an exhaustive guide to get you started. A…
Modernization of Clinical Trials Amidst the Pandemic
This article, written by Kolabtree’s freelance scientist Aditi Kandlur, elaborates on how the pandemic has…
Five Steps to Ensure Data Confidentiality Whilst Hiring Freelancers
In a world where remote working, hybrid workforces and tapping into gig economy by hiring…
AI Trends in MedTech and Digital Healthcare: Kolabtree Whitepaper
Kolabtree have recently published a whitepaper on ‘AI trends in medtech and digital healthcare’, authored…
Six conseils pour constituer et gérer une équipe hybride
Une équipe hybride, composée de ressources à temps plein et d'experts indépendants, pourrait être une...
Mises à jour et tendances MDR - Le guide définitif des réglementations sur les dispositifs médicaux
Il est crucial pour les entreprises de dispositifs médicaux de se tenir au courant des mises à jour opportunes de l'EU MDR, ce qui leur permet...
Les entreprises Medtech pionnières de l'innovation en Europe
Dans la première partie de notre série consacrée aux principaux acteurs du secteur des technologies médicales, des biotechnologies et des soins de santé dans...
Conformité à l'IVDR : 10 conseils pour les fabricants de dispositifs médicaux
Un guide exhaustif de la conformité réglementaire pour les fabricants de dispositifs médicaux de diagnostic in vitro, rédigé par Sundeep Agarwal, expert en...