Why Should You Attend:Once a product goes commercial, measuring the quality, safety, and efficacy attributes of the drug substance and the drug product is crucial. There are well-established ICH guidelines for the validation requirements of typical analytical procedures. In contrast, the requirements for a technical transfer of an analytical procedure from one site to another or within a site to a separate facility are often debated.Areas Covered in the Seminar:ICH guidelines for validation.USP guidelines for validation and verification.Applications of the ICH guidelines for method transfer.Debated topics and approaches.Complex procedures.Establishing boundaries.