After a very unique virtual conference on validation approach, 2nd Annual Cleaning Validation 2022 was deemed as the most successful conference last year, based on the learning potential of the summit. The summit was a mixed workshop and conference model with multiple trainers and experts speaking with live examples and attaching a case study to each presentation.
This year’s in-person summit on validation is dedicated to analysing top-notch recent trends and advanced innovations for more efficient cleaning validation programs. In the manufacturing of medicinal products, the cleaning of facilities and equipment is an important measure to avoid contamination and cross-contamination. In compliance with the EU regulations to GMP Annex 15, cleaning is performed and documented according
to the described procedures.
As we can agree, the Industry is facing a lot of challenges. The Regulatory Agencies are also focusing on cleaning procedures and validation highlighting many gaps.
We, Eminence Business Media, are organizing a two-day in-person conference fully dedicated to the latest developments concerning cleaning validation with a deep focus on the impact of new regulations, automated systems, and best practices learned from real life cases. We have great line of industry experts, 2 workshop leaders, Igor Gorsky and Thomas Altmann and a focused solution provider Leucine Tech, as Platinum Partner, with very apt and relevant solutions for the audience.
Make the most of the opportunity to meet and ask questions to some of the most renowned experts in the field.
Why should you attend?
- Understand the updates on APIC & regulatory guidelines and your existing process.
- How to Build a Robust Cleaning Validation Program
- Learn the practical approach with live case study solutions.
- Identify the best analytical method for meeting quality compliance.
- Network with the industry leaders to understand what they do differently to be successful.
Who Should Attend?
- Managing Directors
- Directors
- Presidents
- Vice Presidents
- AVP’s, Directors
- Sr. GMs, GMs & AGMs
- Site Heads
- Mid Management
from QA/QC Teams, Corporate Quality, Compliance, Manufacturing, and any pharma teams that handle Cleaning Validation and Processes.
