NLM Digital Collections

Search

Search Constraints

Start Over You searched for: Genre Guideline Remove constraint Genre: Guideline

Search Results

121. Unique device identification: policy regarding compliance dates for class I and unclassified devices : immediately in effect guidance for industry and Food and Drug Administration staff

122. Compounded drug products that are essentially copies of a commercially available drug product under Section 503A of the Federal Food, Drug, and Cosmetic Act

125. Requirements for transactions with first responders under section 582 of the Federal Food, Drug, and Cosmetic Act--compliance policy

126. Providing regulatory submissions in electronic format--certain human pharmaceutical product applications and related submissions using the eCTD specifications

128. Measuring the difference: guide to planning and evaluating health information outreach