Location: Webinar

Join us for a comprehensive webinar, that will be conducted in Spanish, designed for Latin American and Puerto Rican GMP drug manufacturing companies, looking to better understand expectations regarding analytical test methods. The analytical methods utilized in cleaning validation need to be qualified as established by the guides such as the FDA Cleaning Process Validation and global cleanliness validation standards for said manufacturing processes. 


This webinar is designed for professionals in pharmaceutical manufacturing who are responsible for high-quality, efficient, cost-effective and compliant medicinal products. 


During this webinar, the following topics will be covered; 


  • Aspects to consider in the selection of analytical methods with a focus on chemical residue

  • Most common analytical technologies for the detection of cleaning agent residues with an emphasis on formulated detergents

  • Acceptance criteria for the validation of the analytical method according to the capabilities of the instrument and particular requirements of the application 


Who Should Attend? Quality Assurance, Regulatory Validation, Quality Control, Operations, Microbiology, Engineering, and Technical Services. 


Click Here to Register