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

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

Siemens’ Closed Loop Quality and Compliance for Medical Devices solution facilitates uninterrupted traceability of the compliance approach, ensuring preparedness for recalls and comprehensive control ...

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

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

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

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

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

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

Proper storage of medical products is critical due to their potential sensitivity to environmental conditions, such as ...

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

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