Sartorius - Manufacturing & Quality Control for Medical Devices

MedTech Intelligence

Volume 15 Issue No. 22


MDIC Advanced Manufacturing Clearing HouseFDA Offers Funding for Adoption of Advanced Manufacturing Technologies

By MedTech Intelligence Staff

Medtech companies can receive up to $300,000 for the adoption of advanced manufacturing technologies through the MDIC Advanced Manufacturing Clearing House. The program is designed to speed adoption and provide guidance for industry and the FDA on the most beneficial applications of advanced technologies.


Rimsys - 2023 MedTech Regulatory Performance Report

Featured Articles


Leveraging AI & ML in MedTech:
Purpose-Built Applications

By Bob Bouthillier, Sunrise Labs

There are several potential applications for machine learning and artificial intelligence in MedTech. In this article, we look at supervised ML with a classifier that learns to correlate IMU data patterns.


Beyond EU MDR:
Unleashing Opportunities to Innovate and Ensure Patient Safety

By Monali Bhansali, Tata Elxsi

The regulatory landscape for medical devices is rapidly evolving, catapulted most recently by European Union Medical Device Regulations (EU MDR). In this article, Monica Bhansali, Practice Lead of Regulatory Affairs at Tata Elxsi, highlights challenges and advancements in the MedTech regulatory landscape, and what the future has in store.


ETQ, LLC, part of HexagonPutting Quality Behind Intelligent Cancer Care
at Varian

Sponsored By ETQ, LLC, part of Hexagon

“A world without fear of cancer” is the corporate mission at Varian, a Siemens Healthineers company. To turn that vision into reality, the oncology care innovator prioritizes automated quality management across its imaging, treatment, and digital solutions. Follow Varian's quality journey from out-of-the-box standard QMS applications to a well-integrated enterprise platform that supports its data-driven product ecosystem with Srinivas Vindula, QMS Project Manager at Varian, and David Isaacson, VP of Product Marketing at ETQ.

Stream Now!

AAMI and BSI Partner to Publish Guidance on Artificial Intelligence

By MedTech Intelligence Staff

AAMI and the British Standards Institute (BSI) have jointly published new guidance documents on performing risk management for machine learning or artificial intelligence incorporating medical devices.

What’s Happening in the UK and Switzerland

By MedTech Intelligence Staff

At the 2023 MedCon Conference in April, Michael Maier, VP of Strategic Regulatory and Quality at Veranex, and James Pink, Director of Medical at Element, provided updates on medical device regulation in Switzerland and the UK.


MedTech Intelligence
November 7-8, Washington DC

SUPPLY CHAIN Intelligence Summit
November 8-9, Washington DC

Abstracts Deadline: June 15

MedTech Intelligence and Axendia are requesting abstracts for content to be presented during our upcoming Conferences.
All abstracts will be judged based on the educational value.


MedTech Library

Terumo Enables Global Collaboration and Clinical Excellence for Groundbreaking Medtech ResearchTerumo Enables Global Collaboration and Clinical Excellence for Groundbreaking Medtech Research

Sponsored By Veeva Medtech

Terumo, global leader in medical technology, transforms to a unified, digital approach to manage global clinical trials and operations. Read this article to learn about the approach, processes, infrastructure changes, and impact on the business.

Drive Healthcare Transformation with Enterprise-Level InfrastructureDrive Healthcare Transformation with Enterprise-Level Infrastructure

Sponsored By Arrow and Dell Technologies

Learn the key considerations and best-fit solutions for healthcare transformation that optimize operations for providers and ensure better outcomes for patients. Discover how the Arrow Electronics and Dell Technologies OEM Solutions portfolio can match any healthcare need.

2023 MedTech Regulatory Performance Report2023 MedTech Regulatory Performance Report

Sponsored By Rimsys

The 2023 MedTech Regulatory Performance Report provides insights and process benchmarks from a survey of 200 medtech regulatory professionals across North America and Europe. The report explores regulatory staffing and team size, workload and average times to complete regulatory projects, compliance issues and costs, and the role of technology and digital transformation.

All Available Resources
Upcoming Events & Webinars

MedTech Intelligence 2023 Washington DC Conferences

More info at

November 7-8
MedTech Intelligence Advanced Manufacturing Conference
Join leading MedTech engineers and manufacturers as we take an in-depth look at the use of advanced manufacturing technologies in quality improvement, speeding time to market and combating labor shortages, and share insights on what’s working, implementation challenges and strategies for successful adoption.

November 8-9
MedTech Supply Chain Intelligence Summit
Gain insight and strategies from procurement professionals, device manufacturers and regulators on how to assess and mitigate risks to the supply chain, improve logistics, and build and maintain a sustainable, resilient supply chain.

November 13-14
MedTech Regulatory Intelligence Summit
The MedTech Regulatory Intelligence Summit brings together RA/QA professionals, device developers and regulators to share experiences and best practices, and find solutions to the key pain points in achieving regulatory compliance throughout the product lifecycle.

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