The electronic Common Technical Document (eCTD) has become the global standard for submitting regulatory information to health authorities, streamlining the process for pharmaceutical and biotechnology companies. While the basic...
In the complex world of drug development, navigating regulatory pathways efficiently can determine how quickly and successfully a product reaches the market. One such pathway in the U.S. is...
TFDA eCTD Specification : The Taiwan Food and Drug Administration (TFDA) has recently released its guidelines for the electronic Common Technical Document (eCTD) format, aiming to standardize and streamline...
