Saudi Arabia
The article provides a general overview of the regulatory approach to be applied concerning biotechnology-based medical devices intended to be marketed and used in Saudi Arabia.
SFDA
The article provides an overview of the regulatory framework for sample collection.
Saudi Arabia
The new article highlights the aspects related to the classification rules applicable to specific categories of healthcare products.
Saudi Arabia
The article provides a general overview of the classification framework for medical devices.
#WednesdayWebinar Join us for our upcoming webinar Global Regulatory Changes to Expect in 2025 January 22, 2025 at 10 AM ET
Register Now
