Task 1. Definition of the protocols for Analytical development, Pharmaceutical development and Stability Test. This is a dynamic Task in the sense that the protocols may be adjusted during the course of the project. As Analytical method the one reported in the official monograph of the USP 34 will be adopted.. - WP2.1 System suitability for the HPLC method reported in USP 34; - WP2.2 Preparation of the working standard; - WP2.3 Set-up of the dissolution test in biorelevant dissolution media. - WP3.1 Definition of the optimal in vitro dissolution profile;
Appears in 2 contracts
Sources: Project Plan, Project Plan