A majority of patients feel lay summaries for clinical trials are very important and won’t participate in future trials if not provided with one...
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A Summarized Report of the Virtual MedTech EU MDR Exchange...
Session summaries from EUMDR exchange conference 2021.
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Which Regulatory Requirements Are Applicable to...
Understanding the requirements for your medical device is vital in today’s market. But are these regulatory requirements applicable to legacy devices?
Navigating the Two-Way Street: 3 Ways to Avoid Dead Ends in HCP...
Today's patients have access to a multitude of resources about their health and condition. HCPs need to find a common ground to make communication...
Ensuring Alignment Across EU MDR Deliverables
How to avoid all these pitfalls and keep thriving in the EU Medical Devices market? Download our handy guide to understand the overlaps in the...
Medical Information in the Digital Age – Quick and Efficient...
Medical Information (MI teams across the pharmaceutical industry respond to product-related medical queries from HCPs, payers, patients, and...
Plain Language in Plain Sight: Why Making it Easier for Patients...
With so many different types of Plain Language Summaries, and the interchangeable terms used for them, patients can often be confused with what...
World Patient Safety Day 2022 – Medication Without Harm
Medication use around the world has increased in the last few years; a 2019 CDC report stated that 48% of respondents who were surveyed mentioned...