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Hosted on MSNOCT Medical Devices 2025: biggest regulatory requirement issues ‘start at the site level’When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...
Siemens’ Closed Loop Quality and Compliance for Medical Devices solution facilitates uninterrupted traceability of the ...
The clock is ticking for medical device and pharmaceutical companies to fulfill their obligations under the Physician Payments Sunshine Act ...
AI was a key theme at OCT Medical Devices 2025, yet human sensibility appears to be the true differentiator in clinical trial ...
China’s State Administration for Market Regulation (SAMR) officially released the Compliance Guidelines on Preventing ...
Technologies announced that it has regained compliance with the Nasdaq Capital Market’s continued listing standard for ...
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
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 ...
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.
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