How To Implement Or Expand USP <922> Water Activity Testing For Oral Solid Dose Pharmaceuticals

The USP<922> Water Activity implementation requires an approach that can give insight into the impact of moisture on critical product quality attributes including stability, dissolution rate, and physical properties of tablets, pills, capsules, and other solid pharmaceutical material.

In this webinar we provide insight on the technical and regulatory justification to add water activity measurements into pharmaceutical stability protocols.