Enhancing manufacturing with process analytical technology (PAT) in 2025
Enhancing manufacturing with process analytical technology (PAT) in 2025
Webinar

Innovation vs. Regulation: Balancing the Pace of Analytical Technological Advancement with Evolving Regulatory Frameworks

Webinar Overview

The pharmaceutical industry has experienced considerable transformation over the past decade, characterized by a notable shift towards biologics and a revived focus on peptide and oligonucleotide drug modalities. It has also witnessed significant changes in the regulatory landscape, particularly with the recent implementation of Analytical Quality by Design concepts. The full ramifications and impacts of these developments on pharmaceutical quality control are yet to be completely ascertained.

In this expert panel discussion, we will explore how this evolving environment, alongside pressing sustainability concerns, drives and fosters innovation in advanced pharmaceutical analytics. We will deliberate on strategies and analytical solutions designed to address the future of quality control, encompassing both the principles of quality and sustainability.

Thursday June 19

05:00 PM CEST

Key Learning Points

  • Evolution of standards and regulatory vision
  • Practical integration of innovative technologies
  • Cross-functional collaboration and lessons learned from other sectors

Who Should Attend

This session is ideal for Scientific Directors, Analytical Science professionals, Innovation and Sustainability leaders, Quality Control Managers, and Regulatory Affairs experts, as well as anyone involved in pharmaceutical development, compliance, or analytical innovation.

Speakers

Registration