In the EU, the AI Act has been approved, carrying significant implications for medical device, technology, and pharmaceutical firms. In the US, ...

Clinical data management companies play a crucial role in the healthcare sector by ensuring the accurate collection, ...

Key highlights included in-depth discussions on regulatory updates and challenges specific to the MEA region, networking ...

India's pharmaceutical industry is set for growth, driven by strong market players, global reputation, and evolving trends.

Americhem, Inc., a globally recognized designer and manufacturer of custom color masterbatch, functional additives, ...

When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...

MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...

In the United States, the biomedical industry encounters numerous regulatory challenges in conducting nonclinical and ...

These strategies can create a healthcare ecosystem that prioritizes patient safety, empowers consumers with information and ...

EQS-News: aap Implantate AG / Key word (s): Regulatory Approval/Miscellaneous Progress in the MDR process - aap receives MDR certificate 27.01.2025 / 14:00 CET/CEST The issuer is solely responsible ...

In this modern era, healthcare organizations face escalating cybersecurity challenges as they transition to digital systems.

Stakeholders also seek a lowering of import duty on medical equipment and policies that encourage R&D in advanced ...