Writing Effective IQ, OQ,PQ Protocols for Equipment Qualification

Instructor: Joy McElroy
Product ID: 705763
Training Level: Intermediate to Advanced
  • Duration: 90 Min
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 obtaining all necessary documents.

recorded version

$299.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Sep-2018

Training CD / USB Drive

$399.00
One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

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 an effective protocols.

Attend this webinar to learn about requirements from regulatory agencies for IQ, OQ, and PQ protocols, examples of deficient protocols. 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.

Areas Covered in the Webinar:

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

Who Will Benefit:

  • Validation Engineers
  • Quality Assurance Personnel
  • Manager and Supervisors
  • Calibration and Maintenance Personnel
Instructor Profile:
Joy McElroy

Joy McElroy
Principle Consultant, Maynard Consulting Company

Upon earning a degree in Zoology at North Carolina State University, Joy McElroy made her debut in the pharmaceutical industry in 1992 at Pharmacia & UpJohn performing environmental monitoring and sterility testing. Her hard work allowed her to move into a supervisory role at Abbott Laboratories where she oversaw their quality control lab. In 1998, Ms. McElroy moved to Wyeth Lederle and worked in quality assurance, performing GMP compliance audits, batch record reviews, and holding annual GMP training for new employees. After working in quality assurance for a few years, she moved into equipment qualification and cleaning validation at Mallinckrodt.

With over 20 years total experience in the pharmaceutical and biotech industries, Ms. McElroy has gained extensive knowledge of quality assurance, process and cleaning validation, equipment qualification, sterilization, and GMP compliance auditing. Her knowledge, experience, and strong work ethic have made her a highly sought-after engineer in both the pharmaceutical and biotech industries.

In 2013, Ms. McElroy started her own company, Maynard Consulting Company, which provides top engineers, auditors, and validation specialist to pharmaceutical, biotech and medical device clients across the United States, Canada, and the world.

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Seminars by Ex-FDA Officials

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email customercare@complianceonline.com call +1-888-717-2436 (Toll Free).

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