Pharmaceutical Manufacturing Equipment Qualification And Maintenance

Instructor: Peggy Kwoka
Product ID: 706208
Training Level: Basic to Intermediate
  • 22
  • April 2020
    Wednesday
  • 10:00 AM PDT | 01:00 PM EDT
    Duration: 60 Min
Attend this webinar to learn about the GMP requirements for pharmaceutical equipment. Regulations require that equipment is to be of appropriate design, constructed not to alter the product, and properly cleaned and maintained. Demonstrating the adequacy of the equipment starts with a risk assessment and a design qualification and continues through installation qualification, operational qualification, performance qualification and process validation. Preventive and corrective maintenance provide assurance that the equipment will continue to operate as intended.

Live Online Training
April 22, Wednesday 10:00 AM PDT | 01:00 PM EDT | Duration: 60 Min

$229.00
One Dial-in One Attendee
$599.00
Group-Max. 10 Attendees/Location
(For Multiple Locations Contact Customer Care)
Super Deal - Get CD/USB Drive Free!

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 48 hrs after completion of Live training

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 after completion of Live training

Combo Offers

Live + Recorded Version

$399.00

Live + Training CD/USB

$499.00

Customer Care

Fax: +1-650-362-2367

Email: customercare@complianceonline.com

Read Frequently Asked Questions

Why Should You Attend:

It is always challenging to manage qualification of equipment in a pharmaceutical manufacturing environment. It is also demanding to know how to document changes and maintenance activities.

In this webinar, you will learn how to base your equipment qualification and maintenance program on a risk management plan and to appropriately document all of the equipment-related activities. Using this risk-based approach, you can streamline the process of addressing equipment failures and managing process changes. You will learn strategies for avoiding common pitfalls and for lifecycle management of manufacturing equipment.

This webinar will provide a risk-based approach from the beginning stages of planning and acquisition of pharmaceutical manufacturing equipment through ongoing usage of the equipment. Planning for and documenting the activities will be discussed. The topic will include the validation master plan, risk assessment, design qualification, installation qualification, operational qualification, performance qualification and the impact of equipment on process validation. Additionally, an understanding of the requirements for preventive and corrective maintenance will be included. You will learn how to set up a preventive maintenance schedule based on risk and when to adjust the schedule to ensure the plan remains suitable.

Areas Covered in the Webinar:

  • The importance of risk management for manufacturing equipment
  • Validation Master Plans
  • Planning for new equipment, commissioning, and completing the design qualification
  • Installation Qualification
  • Operational Qualification
  • Performance Qualification
  • Process Validation
  • Planning for equipment maintenance
  • Documenting equipment maintenance
  • The connection with change control
  • When to revise your equipment maintenance plan

Who Will Benefit:

  • Quality Assurance Director
  • Quality Assurance Management and associates
  • Quality Engineer
  • Operations Manager
  • Maintenance Manager
Instructor Profile:
Peggy Kwoka

Peggy Kwoka
Senior Consultant, Quality GMP Solutions LLC

Peggy Kwoka has more than thirty years of experience in pharmaceutical, cosmetic consumer health and medical device industries including twenty years in Quality Assurance management and consulting. She has managed or provided expertise for more than ten US FDA inspections.

Peggy is currently working with pharmaceutical companies to develop effective quality systems through her consulting firm, Quality GMP Solutions, LLC. She focuses on improving her client’s manufacturing and quality processes to enhance their regulatory compliance profile. She previously held quality assurance management roles at Colgate-Palmolive Company and GlaxoSmithKline.

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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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