March - 20236Managing EditorAlex D'souzaVisualizerChris LynnMichael WayneMarch - 13 - 2023, volume 06 - Issue 19 (ISSN 2691-4093) Published by ValleyMedia, Inc. Emailsales@medicaltechoutlook.comeditor@medicaltechoutlook.commarketing@medicaltechoutlook.comTo subscribe to Medical Tech OutlookVisit www.medicaltechoutlook.com Copyright © 2023 ValleyMedia Inc. All rights reserved. Reproduction in whole or part of any text, photography or illustrations without written permission from the publisher is prohibited. The publisher assumes no responsibility for unsolicited manuscripts, photographs or illustrations. Views and opinions expressed in this publication are not necessarily those of the magazine and accordingly, no liability is assumed by the publisher thereof.*Some of the Insights are based on the interviews with respective CIOs and CXOs to our editorial staffAlex D'souzaManaging Editoreditor@medicaltechoutlook.comMedical devices have always been subject to strict regulation because of the criticality of their usage in maintaining patient health. Recent developments like the FDA's revamped medical device regime, which focuses on clinical decision support software, strengthening cyber security, and more, is increasing the number of mandates medtech manufacturers must comply with. Moreover, the proliferation and development of medical devices have stemmed concerns regarding data security within medical devices since any malicious intent can cause significant disruptions to patient care. Due to these adjustments, restrictions on the use of chemicals in goods, and other laws that apply to electronics, in general, have manufacturers constantly monitor and evaluate regulatory requirements to maintain compliance.Understanding the regulatory risks and actively working to prevent and detect any violations of compliance standards are just some of the processes that medical device firms must adopt to navigate the quickly changing regulatory landscape while minimizing risk. In pursuit of achieving this, organizations are automating their regulatory change management to reduce workload, prioritize routine compliance library reviews, and understand the regulatory risks they are exposed to. Essentially, having the right tools and system support is crucial in maintaining compliance with ever-evolving regulations, which in turn, can help medtech firms increase quality, reduce cost, and decrease time-to-market without compromising innovation.In this edition of MedTech Outlook, we bring you the story of some of the leading medical device regulatory and compliance companies that deliver the best outcome for their clients. This issue also offers a combination of thought leadership articles from Aaron Goodstein, director of quality systems & compliance, MD&D medical safety at Johnson & Johnson, and Oliver Perez, engineering director, process technology and automation at Edwards Lifesciences. The magazine also features Telos Partners as the cover story. The firm takes a highly client-centric approach that combines deep industry knowledge with innovative solutions to help medtech innovators stay in compliance with ever-changing regulations.We hope this edition will provide you with the right assistance in choosing the regulatory and compliance companies that fit your business requirements.Boosting Healthcare Innovations through Holistic ComplianceEDITORIALEditorial StaffJoe PhilipLaura PintoJoshua ParkerMerlin WatsonSarah FernandesGina ClumskyYenny TurnerTiffany Hayworth
< Page 5 | Page 7 >