Use RAMS to power your medical device regulatory activities worldwide

Use RAMS to power your medical device regulatory activities worldwide

Medical Device Regulations and Patient Safety: comprehensive global policy.Подробнее

Medical Device Regulations and Patient Safety: comprehensive global policy.

Short course on the Medical Device Regulation (EU) 2017/745Подробнее

Short course on the Medical Device Regulation (EU) 2017/745

Medical Device Software: Current Developments in the Regulatory WorldПодробнее

Medical Device Software: Current Developments in the Regulatory World

Regulatory Procedures for AI in Medical Devices - Webinar by RSIP Vision September 16Подробнее

Regulatory Procedures for AI in Medical Devices - Webinar by RSIP Vision September 16

why the regulatory intelligence is needed?Подробнее

why the regulatory intelligence is needed?

Short course on Clinical Investigation for Medical Devices and ISO 14155Подробнее

Short course on Clinical Investigation for Medical Devices and ISO 14155

IMDRF - International Medical Device Regulators ForumПодробнее

IMDRF - International Medical Device Regulators Forum

Discover RAMS - medical device regulatory intelligence softwareПодробнее

Discover RAMS - medical device regulatory intelligence software

What "Exempt" Means with Respect to Medical Devices & RegulatoryПодробнее

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Understanding Biocompatibility in Medical DevicesПодробнее

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Argentina- Medical Device Registration- ANMATПодробнее

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How to Register Medical Devices in the UAEПодробнее

How to Register Medical Devices in the UAE

3 easy steps to establishing a quality and regulatory strategy for your medical device (Scope phase)Подробнее

3 easy steps to establishing a quality and regulatory strategy for your medical device (Scope phase)

BSI Standards e-Conference: Regulatory and standardization challenges for connected medical devicesПодробнее

BSI Standards e-Conference: Regulatory and standardization challenges for connected medical devices

Medical Device RegulationПодробнее

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WEBINAR: Medical devices software development and applicationsПодробнее

WEBINAR: Medical devices software development and applications

Global Medical Device and IVD Regulatory Changes in 2020 and Their Impact to Asia Pacific.Подробнее

Global Medical Device and IVD Regulatory Changes in 2020 and Their Impact to Asia Pacific.

Medical Device Regulation in a Post Brexit WorldПодробнее

Medical Device Regulation in a Post Brexit World