Health Canada Draft Guidance on Significant Changes: Types of Changes
The new article describes specific types of changes to medical devices in detail and outlines the critical points related to the regulatory status thereof.
The new article describes specific types of changes to medical devices in detail and outlines the critical points related to the regulatory status thereof.
The article highlights the critical points related to the concept of significant changes in the context of medical devices allowed for marketing and use in Canada.
The new article describes in detail the regulatory approach to be followed when reviewing the applications related to clinical investigations to be conducted in Pakistan.
The new article highlights the critical points related to the application process, outlining the key steps to be taken when applying for approval in a clinical investigation.
The new article describes in detail the key responsibilities of the parties involved in clinical research.
The article provides a general overview of Pakistan’s regulatory requirements for clinical research.
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