Webinar on FDA Regulations for Environmental Monitoring(EM) Program

Overview: 

Upon completion of this training, you will be able to Describe how Clean room Environmental Monitoring (EM) Program fits into the Regulations. Explain the basis of the Four (4) Phases of Clean room transitional monitoring (Pre-qualification through post-qualification EM) and what each type stands for. List the basic content of a well-designed, effective and compliant EM Program. Explain the relationship between an EM Excursion Program and CAPA

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?

Who Will Benefit:

• Quality Control,
• Quality Assurance
• Microbiologist, Facilities
• Chemist, Analysts
• Manufacturing

Speaker Profile: