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Regulatory Submissions

Regulatory Submissions (510(k), MDL, Technical Documentation)

Regulatory Submissions (510(k), MDL, Technical Documentation)

Medical practitioners, give your patients the best in state-of-the-art technologically advanced medical devices that are both safe and effective. Our goal is to help bring a medical device to the market in a streamlined manner, ensuring your medical devices meet all regulatory affairs requirements set forth by various medical agencies. Here at Global RQC Med Device Solutions LLC (Global RQC), we provide medical device regulatory affairs services to the medical industry.

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Regulatory Affairs for Medical Devices

Our primary objective is to help manufacturers achieve regulatory clearance, quality system development, as well as regulatory compliance for new medical devices. We also aim to ensure medical practitioners are provided with the most suitable devices for providing superior patient care. Contact us to learn more about our medical device quality consulting and regulatory services.