FAQs by Year: 2022
Cybersecurity in Medical Devices
Understand cybersecurity requirements for medical devices in this comprehensive FAQ.
FAQs about the Saudi Arabia Electric Vehicles Programme
Explore the compliance standards for electric vehicles as defined by the Government of Saudi Arabia.
FAQs about the Egypt ECAP Programme
Learn about Egypt's ECAP programme and the required compliance standards for businesses.
Cybersecurity in Medical Devices
Explore FAQs on cybersecurity measures for medical devices and regulatory compliance.
FAQs about the Iraq CAP Programme
Find information on the Iraq CAP programme and related compliance standards in this FAQ.
FAQs about the Ghana EasyPass Programme
Get details on the EasyPass programme from the Government of Ghana and its compliance needs.
FAQs about the Ivory Coast VoC Programme
Understand the VOC programme compliance requirements from the Government of Ivory Coast.
FAQs about the Gabon PROGEC Programme
Learn about the PROGEC programme and its compliance requirements from the Government of Gabon.
FAQs about the Cameroon PECAE Programme
Get information on the PECAE programme from the Government of Cameroon and its compliance needs.
Warnock Hersey (WH) Mark FAQ
The Warnock Hersey (WH) Mark is North America’s leading product safety and performance mark for building and construction products. Learn more with our FAQ sheet.
Greenhouse Gas Phase 2 FAQs
Explore automotive GHG2 testing standards and requirements in this FAQ.
FAQs about the Saudi SALEEM Programme
Find details about the Saudi Saleem programme and its compliance requirements here.
FAQs about the Saudi Cosmetics and Perfumery Products Programme
Get insights into the Saudi Cosmetics Programme and its compliance standards in this FAQ.
FAQs about the Egypt Food Programme
Access information on food safety and compliance standards in Egypt in this FAQ.
IEC 62304 Medical Device Software Life Cycle Processes | FAQ Sheet
IEC 62304 is an international standard for the development and maintenance of software used in medical devices. It outlines the processes and lifecycle stages required to ensure that software used in medical devices is safe, reliable, and effective throughout its entire lifecycle.