OVERVIEW

Cleaning Validation Summit 2024 is organized by Uventia Global s.r.o. and will be held from Oct 01 - 02, 2024.

Conference Overview:
Drug products and active pharmaceutical ingredients (APIs) may be contaminated by other drug products or APIs, raw materials, intermediates, cleaning aids, microorganisms, particles and other materials. Contamination causes costly raw materials to be scrapped, triggers regulatory actions and, most importantly, endangers the safety of patients.

In order to avoid contamination of the product, robust cleaning procedures must be performed. Our online meeting facilitates peers’ reflection and discussion on approaches to establishing and revising CV programs to meet regulatory requirements, verifying CV protocols and preventing ineffective or incorrect approaches to cleaning validation programs, risk based cleaning validation, selecting the right equipment/cleaning procedure combinations, testing for API residues and calculating residue limits, considerations on combining cleaning and sanitization, finding and developing practical analytical methods and sampling procedures.

Be a part of our webinar sessions to build practical and compliant cleaning validation program and ensure that the quality of your next product is not affected by contamination.

We Will be Focusing on:
• QRM in Cleaning Validation
• Cleaning Validation in shared facilities
• Product bracketing and equipment grouping during Cleaning Validation
• CIP Cleaning process optimization and sustainability
• Maintaining the Cleaning Validation program
• Regulatory and GMP aspects for Cleaning Validation
• Developing suitable analytical methods
• Sampling methods and sampling recoveries
• Establishing acceptance limits
• Selection of Cleaning agents
• Visual inspection for Cleaning Validation
• Microbiological aspects of Cleaning Validation