US EDITION - SETTING DRUG PRODUCT SPECIFICATION MASTERCLASS
06-08 OCTOBER, 2025
Navigate regulatory submissions with confidence
ONLINE MASTERCLASS | 06-08 OCTOBER, 2025
Starting time: BST 13:00 p.m.
Overview
In this Masterclass, youll move beyond regulatory checkboxes to mastering science-driven, globally compliant specifications that ensure drug product quality and patient safety. Regulatory scrutiny is increasing, and poorly justified specifications can lead to delays, rejections or worse recalls.
By the end of this Masterclass, you wont just know HOW to set specifications youll understand WHY they matter and how to use them to create a strategic advantage in regulatory submissions and product lifecycle management.
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Who should attend?
-Pharmaceutical Regulatory Affairs professionals
-Analytical scientists
-Quality Control and Quality Assurance specialists
-CMC and Formulation development experts