US EDITION - SETTING DRUG PRODUCT SPECIFICATION MASTERCLASS

06-08 OCTOBER, 2025

Navigate regulatory submissions with confidence

SETTING DRUG PRODUCT SPECIFICATION MASTERCLASS - US EDITION

ONLINE MASTERCLASS | 06-08 OCTOBER, 2025

 

Starting time: BST 13:00 p.m.

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masterclass in pharma

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.


#masterclass #qaqchub #pharma #qualityassurance #qualitycontrol #drug #specification

Who should attend?

-Pharmaceutical Regulatory Affairs professionals
-Analytical scientists
-Quality Control and Quality Assurance specialists
-CMC and Formulation development experts

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Testimonial

Our success stories

"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"

Aurelie Vivicorsi
USP PD Team Manager
Celonic AG
Switzerland

Our success stories

"High attention to detail in course content and very well delivered"

Simon Halsey
Product Development Manager
Essentra Packaging
United Kingdom

Our success stories

"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"

Emilia Szwej
Manager, Senior Investigator
MT Sword Laboratories (BMS)
Germany

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