
HSA Draft Guidance on Clinical Evaluation: Data Sources
The new article addresses the aspects related to the sources of data used in the context of clinical evaluation of medical devices.
The new article addresses the aspects related to the sources of data used in the context of clinical evaluation of medical devices.
The new article addresses the aspects related to the key concepts used in the context of clinical evaluation.
The new article highlights the aspects related to the general principles of clinical evaluation.
The article provides a brief overview of the regulatory requirements in the sphere of clinical evaluation of healthcare products.
The new article highlights the aspects related to the information to be included in the submissions with respect to manufacturing processes and sites involved. Table of Contents The Health Sciences Authority (HSA), a Singapore’s regulatory agency in the sphere of...
This article highlights key medical device regulations to know in 2023 and their implications for the industry. Table of Contents In the ever-evolving landscape of healthcare, medical device regulations play a vital role in ensuring the safety, efficacy, and...