The Evolution and Promise of Pharmacogenomics
in Precision Medicine

By Hidaya Aliouche

While pharmacogenomics has traditionally been the domain of academic research, policymakers are now showing a burgeoning interest in its potential to enhance patient outcomes and mounting evidence from the pharmaceutical industry is fuelling interest in this field.

Misconceptions of Miniaturization:
Smaller is Better

By Nicholas Lesniewski-Laas, Sunrise Systems

Product developers need to understand the technical challenges in device miniaturization but should be careful not to go beyond what is needed for the product. Sometimes further miniaturization is critical to the success of a product, sometimes it is superfluous, and sometimes it is even detrimental.

CDRH Releases New Dataset for Biocompatibility of Medical Devices

By MedTech Intelligence Staff

“In the future, CDRH intends to increase the breadth of the dataset of chemicals and RRF information it makes publicly available, and to add other detection methodologies such as liquid chromatography (LC).”

Flex Recognized as a 2024 World’s Most Ethical Company

By MedTech Intelligence Staff

“Companies that operate with business integrity elevate industry standards and perform better in the long-term. We are impressed with Flex's continued focus on ethical business practices, and dedication to making a real impact for its stakeholders.”

FDA Medical Device Sterilization Town Hall Series Continues April 29

By MedTech Intelligence Staff

The FDA is hosting it next town hall on medical device sterilization on April 29. The session will include discussion on topics and formats for future sessions in the series.

Please visit the newest MTI Resource Center
Post-Market Surveillance

The MTI Post-Market Surveillance Resource Center provides current news and information specific to maintaining medical device post market product quality & compliance. PMS is a critical component in achieving global Regulatory Excellence to ensure medical devices remain safe, effective, and reliable for end-users.

Bookmark this page for future reference!

Sponsored By

Leveraging Technology to Optimize MDR Compliance Outsourcing & Partnership

Download this case study for insights on optimized regulatory processes via tech-enabled services from Celegence. Acumed made their MDR compliance a success by boosting efficiency, saving time, and streamlining collaboration.

Download to learn more

How redesign can help meet sustainability demands for medical devices

The ultimate guide to the EU MDR and IVDR GSPR, 2nd Edition

5 eSTAR Challenges MedTech Regulatory Teams Must Overcome

How to Achieve Optimal Weighing Performance with Lab Balances

Better device outcomes through better data

The Emergence of Lateral Flow Assays in Diagnostics

Terumo Enables Global Collaboration and Clinical Excellence for Groundbreaking Medtech Research

Drive Healthcare Transformation with Enterprise-Level Infrastructure

2023 MedTech Regulatory Performance Report