The article addresses the key points related to the pathology peer review for a specific type of nonclinical investigation. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has...
The new article highlights the aspects related to the actions taken by the applicant and their impact on the review clock and timelines. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare...
The article provides an overview of the performance goals related to the applications under the premarket approval framework. Table of Contents The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has...
The new article covers the aspects related to the application of the reliance approach to specific categories of healthcare products and also provides an overview of the reliance procedures. Table of Contents The Drug Regulatory Authority of Pakistan (DRAP), a...
The article provides a general overview of the approach to be applied with respect to the review clock in the context of applications for marketing approval. The document also describes the main regulatory actions to be taken by the authority based on the application...