The Blanket No Change Certification was introduced in 2017 when the FDA published the ‘Final Labeling Rule’: Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs. This rule requires any organization selling drug products in the US to electronically register (annually) the drug products and assign an NDC Code to the product. Reed Tech hosted a webinar, October 13, 2020, discussing the annual Blanket No-Change Certification submission requirements for drug product listings and what is needed to complete the process. The discussion specifically focused on the five steps necessary to create a successful submission, invaluable tips and audience Q&A.
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