Business people looking through a futuristic digitally generated display
15th Anniversary Issue:
Reframe – Reset – Reimagine

Welcome From Martin Lush

This edition is special for the NSF team. We’re celebrating 15 years of the Journal and it’s also our first exclusively digital edition. We hope you enjoy our new format and take away useful information.
Male and female researchers dress in scrubs in front of a microscope - Time to Reset – For 2021 and Beyond | NSF

Featured

Time to Reset - For 2021 and Beyond

NSF’s health sciences experts share what they’ve learned over the last year across pharma, nutritional supplements, medical devices and IVDs, and how COVID-19 forced us to think differently. They also reflect on how we can move forward.

At a Glance

Celebrating 15 Years of the Journal
Hear from our experts, past and present, who have been involved in the Journal.
Celebrate with us
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Regulatory Updates

EU, ICH and Brexit Pharma Regulatory Update - July 2020 to January 2021

By Peter Gough

Updates to U.S. FDA Legislation and Guidance – Fall 2020

Key Updates on the European Medical Device Market – October to December 2020

By Lukas Block

U.S. Medical Devices Regulatory Update – October to December 2020

By Deborah Baker-Janis

News From NSF

Green, pink, blue and yellow pills on a white background - NSF Provided Complimentary Pharma Training to UK NHS Staff | NSF

NSF International Provided Complimentary Pharma Training to UK NHS Staff

Graduates from QP's alumni group shot - NSF’s 2020 Virtual QP Alumni Event Raises £3,950 for Charity | NSF

NSF’s 2020 Virtual QP Alumni Event Raises £3,950 for Charity

Adoption of AI and Digital Solutions in the MedTech Industry

MedTech Summit in association with NSF conducted one of the biggest surveys of its kind in November 2020 across medical device and IVD professionals around the world to understand where the MedTech industry is in its journey toward digitalization.
Get the key insights
Medical Devices Regulatory Q&A Session
NSF experts Oliver Christ, Kim Trautman and James Pink host a Q&A session to answer your questions on topics including the EU MDR, the regulation in relation to COVID-19 and quality management systems.

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