Medical device companies have to deal with continuous changes ... According to a survey sponsored by Genpact, 72.0% of executives from the life sciences industry consider regulatory compliance to be ...

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

Speaking on a panel during the Outsourcing Clinical Trials (OCT) Medical Devices 2025 conference ... during a clinical investigation, regulatory compliance is only as good as the data input.

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

China’s State Administration for Market Regulation (SAMR) officially released the Compliance Guidelines on Preventing ...

Siemens’ Closed Loop Quality and Compliance for Medical Devices solution facilitates uninterrupted traceability of the ...

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

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

AI was a key theme at OCT Medical Devices 2025, yet human sensibility appears to be the true differentiator in clinical trial ...

The MHRA has issued guidance to help manufacturers ensure that digital mental health technologies are effective, reliable and safe.

From conferences to workshops to expo floor education, MD&M West has an educational agenda with something for all.