Overview: In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sound process validation program in order to develop and implement bulletproof solutions that are accepted, effective, and efficient. Through case study analysis we will examine best practices to provide thoughts and ideas to develop or improve the performance of your current system.Why Should You Attend:The cost of non-compliance is therefore more than that of compliance. Are you in compliance with the FDA regulations for Cleaning Validations of your manufacturing equipment?Areas Covered in the Session: Understand the importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the productUnderstand the FDA perspectives on cleaning validation and areas of concern during regulatory inspectionsBe able to set up cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulationsPrepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agenciesWho Will Benefit:Senior quality managersQuality professionalsProduction supervisorsValidation engineersProcess ownersQuality engineersQuality auditors