Due to the high number of questions we received at the Virtual MedTech Summit in October, we have decided to run a follow-up Q&A session with our experts. Join the live session for free to get all your MDR, IVDR and QMS questions answered. Register now: www2.nsf.org/l/129231/2020-…

Our IVD expert Robyn Meurant shares her thoughts on the long-awaited EU IVD Classification Guidance, including her concerns on what may be missing. Read the full Pharma intelligence, informa article below. pharmaintelligence.informa.com/products-and-s…

Participe do seminário com a NSF International e as associações ALADDiV, Anbiotec Brasil e CBDL e fique sabendo sobre as mudanças relevantes para empresas exportadores e importadores. Link para inscrição: www2.nsf.org/l/129231/2020-…

There is a right way (and a wrong way) to go about quality systems remediation. Learn more about NSF International's remediation resources and how we can help your company evaluate, rework and improve your quality systems: lnkd.in/dRzn2nm

Following their presentations at the MedTech Virtual Event in October, NSF experts Oliver P. Christ, Kim Trautman and James Pink answer your questions on topics including the EU MDR, the regulation in relation to COVID-19 and quality management systems. youtube.com/watch?v=RI3-dK…

In the biggest of its kind, MedTech Summit in association with NSF International conducted a survey across medical device and IVD professionals to understand where the MedTech industry is in its journey towards digitalisation. Read the full report: informa.turtl.co/story/medtech-…

On January 7th, join us as Dr. Kazem Kazempour, President at Amarex Clinical Research, LLC, details enrichment strategies for clinical trials. Learn more and register today: lnkd.in/gNYfj68 #clinicaltrials #clinical #enrichmentstrategies #enrichment #webinar

Demonstrate compliance. Learn what a regulator expects to see during an inspection and be prepared: lnkd.in/ddR3kQG

Did you know? Both the FDA and EMA have the highest number of import bans/non-conformance reports from sites in India. Check out this document for more insights and contact [email protected] if you need immediate consultation: bit.ly/2JDL0Zj

NSF experts part of a global panel addressing the current state of EU MDR and evolving issues. bit.ly/369eRBi Wednesday, February 3, 2021, 10:00am - 2:00pm ET Thursday, February 4, 2021, 10:00am - 2:15pm ET #eumdr #medicaldevice

“The pharma industry can move fast when it must!” Check out this and more insights from the #pharma and medical device experts at NSF International in the latest issue of Health Sciences Journal: bit.ly/2OqWVMh #COVID19 #medicaldevices

A Paradigm Shift in Diagnostics Regulation is Coming, Ready or Not. An article featuring Robyn Meurant provides insight into the current state around IVDR and some of the future challenges. Credit: MedTech Strategist - Market Pathways bit.ly/2ZlrzsT

Register now for our complimentary keynote lnkd.in/dg7QWyQ * Update on the most relevant changes * Benefit from our experience gained through implementation projects #IVDR #IVD #medicaldevices #medicaldevice #medicaldeviceregulation #MedTech

A Paradigm Shift in Diagnostics Regulation is Coming, Ready or Not. Insight into the current state around IVDR and some of the future challenges. Credit: MedTech Strategist - Market Pathways bit.ly/2ZlrzsT #IVDR #IVD #MedicalDevices #MedTech

Join us in March and learn how to plan and conduct internal audits in-line with regulation (EU) 2017/745 for medical devices. Participants will also complete our five-star rated two-hour eLearning“EU MDR – A Comprehensive Overview”. Register online: nsfmedicaldevices.trainingfolks.com/store/1024229-… #EUMDR

This interactive two-day course describes the regulation from an auditors' perspective and will provide you with practical instruction to plan and conduct internal and supplier audits based on our EU IVDR model. Register your place online: nsfmedicaldevices.trainingfolks.com/store/1024204-… #euivdr

Join us on April 13-14 for this interactive training and get an in-depth understanding of the risk management and design/development regulatory requirements relative to FDA’s 21 CFR 820, ISO 13485:2016 and EU MDR. Course details: nsfmedicaldevices.trainingfolks.com/store/1024219-…

In this white paper, former FDA Investigator Robert Ruff provides a behind-the-scenes look at how FDA medical device inspections are planned, conducted and managed. View online; nsf.org/knowledge-libr… #FDA #medicaldevices

Led by expert Robert Ruff, this #medicaldevices course will benefit quality professionals responsible for managing and facilitating #FDA inspections and those responsible for defining, implementing and maintaining an effective quality management system. nsfmedicaldevices.trainingfolks.com/store/1024246-…

Learn more about NSF's #eumdr eLearning. As the deadline to meet the new EU regulation approaches and products become certified under more stringent requirements, we are here to help you succeed. eLearning details: nsfmedicaldevices.trainingfolks.com/store/393955-e… youtube.com/watch?v=qI_4na…