This equipment qualification webinar will discuss the requirements for IQ, OQ, and PQ protocols. It will train about the various components of each protocol, Proper language for documenting qualification testing including how to Collect data, conduct tests, and obtain all necessary documents.

Areas Covered:-

• Regulatory Requirements for writing IQ, OQ, PQs
• Components of an effective IQ, OQ, and PQ
• The proper language used to author protocols and document test results
• Collecting Data
• Conducting Tests
• Protocol Templates
• Writing generic IQ, OQ, and PQ protocols
• Obtaining necessary documentation

Frequently Asked Question:-

• Do you recommend separate documents for each Qualification Process?

Why Should You Attend:-

Regulatory Agencies expect Pharma, Biologics, and Medical Device manufacturers to maintain control over their equipment. The FDA and various other regulatory agencies are finding deficiencies with the qualification of analytical and manufacturing equipment. A large number of the deficiencies occur due to poorly written IQ, OQ, and PQ protocols. Proper equipment qualification cannot occur without effective protocols.

Attend this webinar to learn about requirements from regulatory agencies for IQ, OQ, and PQ protocols, examples of deficient protocols. The components of each protocol will be discussed in depth. Proper language for documenting qualification testing will be discussed including methods of Collecting data, conducting tests, and obtaining all necessary documents.

Who Should Attend:-

• Validation Engineers
• Quality Assurance Personnel
• Manager and Supervisors
• Calibration and Maintenance Personnel