M&As: Maximizing the Partnership Process
on Both Sides

By Leslie Storms, Ethicon, Martha Shadan, Miach Orthopaedics, and
Kristine Iliara, Smith+Nephew

Leslie Storms, U.S. president of Ethicon, Martha Shadan, CEO of Miach Orthopedics, and Kristine Ilaria, vice president of Corporate Development at Smith+Nephew, share lessons learned from their panel “Making Acquisition Strategy Succeed: Perspectives from Both Sides of The Deal.”

Predictive Quality for Medical Devices

Sponsored By Critical Manufacturing

Wouldn’t it be great to know and be able to automatically release products when every process stayed within the specified envelope? And to sample or test only as much as a particular process requires, no more or less? Those are the promises of predictive quality. Get to know what executives from Medtronic, B Braun, Jabil and Ultradent have to say about it.

Download to learn more

FDA Announces Funding Opportunities for Medical Device
Development Tools

By MedTech Intelligence Staff

The MDDT program was developed in collaboration with the National Institutes of Health’s (NIH’s) National Institute of Drug Abuse (NIDA), National Institute of Dental Craniofacial Research (NIDCR) and National Cancer Institute (NCI) as a way for the FDA to qualify tools that medical device sponsors can use in the development and evaluation of medical devices.

Raising the Bar on Quality for MedTech Production

By Mohamed Benkirane, Critical Manufacturing

Inspecting for quality after a process is completed is reactive and outdated. Instead, the future lies in predicting quality and quality issues. For medical device manufacturers, the advantages in predictive quality are so great they simply cannot be ignored.

Realizing the Promise of Quality Automation
How Symmetry Surgical Increased Efficiency, Reduced Compliance Risk & Increased Awareness thru Quality Process Automation

Sponsored By ETQ, LLC, part of Hexagon

Tracy Newton Mapes, Sr. Director of Quality at Symmetry Surgical, shares best practices and lessons learned in Symmetry Surgical’s journey to incorporate Quality Automation.

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Streamlining the Literature Review Process

By MedTech Intelligence Staff

Peter O’Blenis, CEO of Evidence Partners, discusses the growing role—and challenges –of literature reviews in the medtech market.

Veranex Acquires Medidee

By MedTech Intelligence Staff

The acquisition expands Veranex’s European footprint as well as the scale and scope of its clinical studies capabilities.

Featured Quote

Many graduates finished school in a remote learning environment and were denied the opportunity to experience in-person internships, a key factor in acclimating to an office setting. Organizations should take responsibility for introducing these new hires to a different way of working.

— Leon Hendra, Real Staffing Group

Increase agility and innovation with PLM for medical devices

Sponsored By Siemens

Siemens PLM for medical devices is an integrated end-to-end product development system that tackles complexity and regulation through re-use, content capture and collaboration.

The Impact of Covid-19 on the Medical Device Supply Chain

Sponsored By Loftware

It’s no secret, the medical device supply chain was significantly impacted by the COVID-19 pandemic. Discover how leading medical device manufacturing companies adapted to meet the changing demands with labeling to ensure uptime.

Adapting to COVID-19 with simulation in the medical device industry

Sponsored By Siemens

Learn how medical device manufacturers are using simulation to enhance their design process to help fight COVID-19 and continuously innovate.

6 Requirements for Medical Device Manufacturers in 2022

Sponsored By Rootstock Cloud ERP

Discover the 6 key requirements to consider when executing your digital transformation strategy and learn how to turn uncertainty and disruption into a model for sustainable growth.

Preparing for Europe’s New Medical Device Regulation:
The Essential Guide to EU MDR Compliance

Sponsored By PTC Arena

Download our whitepaper today as we provide the key steps to making a successful MDR transition, as well as some insights on how an enterprise quality management system (eQMS) solution can help simplify compliance.

Launching your medical device:
A strategy & execution cross-functional guide

Sponsored By Definitive Healthcare

Data Curation: Enabling your Digital Strategy with a Comprehensive Data Strategy

Sponsored By Innovaccer

7 Principles of Product-Centric Quality Management:
A Guide for Medical Device Innovators

Sponsored By PTC Arena

Unified Medical Imaging Solutions:
The Next Evolution in Imaging

Sponsored By Arrow and Dell Technologies

The Rise of Implantable Devices

Sponsored By AMETEK-COINING

Medical device design control with Siemens Digital Industries Software

Sponsored By Siemens

The Post-Market Gambit: After EU MDR and IVDR:
A Systematic Compliance Framework for Driving MedTech Innovation

Sponsored By Huma.AI

How to Address the Top Four Labeling Challenges Facing Medical Device Manufacturers

Sponsored By Loftware, Inc.

The Ultimate Guide to Next-Generation Supplier Management

Sponsored By ComplianceQuest