COURSE ID 1808

IQ, OQ, PQ

AVAILABLE On-demand
12 Hours

On-Demand

Offering Price
$ 2330
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Team Training

When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.

Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.

In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.

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Remember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.

Executing Installation, Operational and Performance Qualifications in Support of Process Validations
The Installation/Operational/Performance Qualification of equipment, systems and facilities for sterile, oral solid dosage forms, liquids, finished and bulk drugs in the Pharmaceutical and Bio Pharmaceutical manufacturing operations are essential parts of the overall validation process. Equipment and systems must be installed, operated, and maintained within design specifications and facilities must be accepted as fit for use. Lastly, processes must be shown to be reliable and robust to assure the consistent quality and integrity of the final product.

This 12-hour accredited ON DEMAND training provides a basic and thorough understanding of preparing, executing, reviewing, and approving qualification protocols. A Risk Based approach to impact critically assessment is also provided along with an overview of ICH Q9 Quality Risk Management and ASTM E 2500 approaches now being applied by the industry.

Though no library of completed protocols will be provided, examples and workshops will be utilized to enhance learning , Executing Installation, Operational and Performance Qualifications in Support of Process Validations. The Installation/Operational/Performance Qualification of equipment, systems and facilities for sterile, oral solid dosage forms, liquids, finished and bulk drugs in the Pharmaceutical and Bio Pharmaceutical manufacturing operations are essential parts of the overall validation process. Equipment and systems must be installed, operated, and maintained within design specifications and facilities must be accepted as fit for use. Lastly, processes must be shown to be reliable and robust to assure the consistent quality and integrity of the final product.

This 12-hour accredited training provides a basic and thorough understanding of preparing, executing, reviewing, and approving qualification protocols. A Risk Based approach to impact critically assessment is also provided along with an overview of ICH Q9 Quality Risk Management and ASTM E 2500 approaches now being applied by the industry. Though no library of completed protocols will be provided, examples and workshops will be utilized to enhance learning.

This introductory/intermediate course is designed for individuals who need a basic, but thorough understanding of the Installation/Operational/Performance Qualification Process for equipment and systems in support of Process Validation for the manufacture of regulated products. The course will benefit individuals in:

– Engineering
– R&D
– Technical Services/Validation
– Regulatory Affairs
– Quality Control/Assurance
– Production

course instructor

Charlie Neal
Owner and Senior Consultant for Premier Quality Consulting

Charlie Neal’s Courses
Charlie Neal, Jr., Owner and Senior Consultant for Premier Quality Consulting, has been in the Pharmaceutical industry for over thirty-five years. He has a wealth of hands-on technical experience acquired from the chemical, drug, device, and pharmaceutical industries. His experience crosses into many areas of these industries including Research, Development, Process Engineering, Validation, Technical Transfers, Manufacturing, Quality, Compliance, Project Management and Sales and Marketing. Mr. Neal has written and presented numerous papers on Qualification and Validation and their requirements in the Life Science industry. His expertise was further expanded while an active member of the Institute of Validation Technology's Editorial Board. Mr. Neal has written and published articles on Technology Transfers and has presented on these topics internationally, including in Tokyo, Japan. He has authored a chapter on Transdermal Process Validation that was published in the 3rd edition of Pharmaceutical Process Validation. His company, Premier Quality Consulting was established to offer consulting expertise to the Pharmaceutical and Bio-Tech companies.