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

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, validation, and analysis of clinical trial data. Their work enhances research ...

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 ...

In the wake of the 2024 U.S. elections, stakeholders in the life sciences and health care industry are intensely focused on the policy ...

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

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 ...