THE IMPORTANCE OF GMP AUDITS IN ENSURING PRODUCT SAFETY AND QUALITY


Why NextGen eCTD Is Key to Faster, Smarter Drug Approvals

In the fast changing pharmaceutical landscape, speed and accuracy in regulatory submissions can be the difference between success and failure of a new drug. For years, the traditional Electronic Common Technical Document (eCTD) format has been the backbone of regulatory filings, but as the industry and global standards have become more complex, the

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