Home) Article Index) Subjects) Validation and regulatory compliance Tablets & Capsules is the only technical publication devoted exclusively to readers in the tablet and capsule processing industries.

		Books Dissolution Theory, Methodology, and Testing Handbook of Dissolution Testing, Third Edition Pharmaceutical Dissolution Testing Eye on Excipients Eye on Excipients: IPEC meeting Eye on Excipients: Third-party auditing Spotlight on Nutraceuticals Spotlight on Nutraceuticals: Clearing the regulatory hurdles to bring a supplement product to market Technical Articles Assessing an analytical method for the dissolution profile of an extended-release tablet in accordance with QbD Compliance challenges facing the nutraceutical and dietary-supplement industries Consistency, conformity keys to vanquishing validation woes Containment of high-potency drug products: Outsourcing and other challenges Contracting with the dietary supplement cGMPs in mind Dispelling solid dosage misinterpretations of the USP-NF Environmental monitoring systems: Overview and the path toward validation Gaining reassurance from third-party auditing How to validate a tablet press Mixing and cleaning efficiency of a 200-liter perforated coating pan equipped with shark fin baffles New ADIs and GMPs spell C-H-A-N-G-E Responses to the final GMP rule for dietary supplements Rethinking stability testing for tablets and capsules in containers The new dietary-supplement GMPs: An invitation to science The role of the ingredient supplier in cGMP compliance USP's offers toolkit for dissolution laboratories Validation of dissolution test procedures