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Emergo by UL's new human factors tool - provides training, tools, and resources.

Our software tools offer digital regulatory monitoring for medical device compliance and access to human factors engineering tools.

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TalkingPoints is a round-up of news, insights, and resources about human factors and usability for medical devices, IVDs, combination products, and more.

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Process Charts

Visualize your path to product registration with our intuitive, high-level guides.

All regulatory process charts are available to download in Regulatory Affairs Management Suite (RAMS).
Get your first chart for free when you create a RAMS account.

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Process Charts

All regulatory process charts are available to download in Regulatory Affairs Management Suite (RAMS).
Get your first chart for free when you create a RAMS account.

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Taiwan Medical Device Regulations

India Medical Device Regulations and Approval

European In Vitro Diagnostic Devices Regulation (IVDR) CE Marking Regulatory Process

Comprehensive Guide to FDA Clearance for Your Medical and IVD Device

Japanese Regulatory Approval Process for Medical Devices

Australian TGA Regulatory Approval Process for Medical and IVD Devices

Chinese NMPA Regulatory Approval Process for Medical and IVD Devices

EU MDR CE Marking Certification Process

Saudi Arabia (SFDA) Medical Device Regulations

Malaysian MDA Medical Device Regulations

Singapore Medical Device Regulations

Costa Rica Regulatory Approval Process for Medical and IVD Devices

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Process Charts

All regulatory process charts are available to download in Regulatory Affairs Management Suite (RAMS). Get your first chart for free when you create a RAMS account.

Filter by Loading...

Filter by

Taiwan Medical Device Regulations

India Medical Device Regulations and Approval

European In Vitro Diagnostic Devices Regulation (IVDR) CE Marking Regulatory Process

Comprehensive Guide to FDA Clearance for Your Medical and IVD Device

Japanese Regulatory Approval Process for Medical Devices

Australian TGA Regulatory Approval Process for Medical and IVD Devices

Chinese NMPA Regulatory Approval Process for Medical and IVD Devices

EU MDR CE Marking Certification Process

Saudi Arabia (SFDA) Medical Device Regulations

Malaysian MDA Medical Device Regulations

Singapore Medical Device Regulations

Costa Rica Regulatory Approval Process for Medical and IVD Devices

Request information from our specialist

Thank you! We've received your request.

All regulatory process charts are available to download in Regulatory Affairs Management Suite (RAMS).
Get your first chart for free when you create a RAMS account.