ComplianceOnline

Analytical Instrument Qualification-Understanding the New USP draft Chapter

Instructor: Dr. Ludwig Huber
Product ID: 700885
  • Duration: 90 Min

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

Training CD

$500.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-565-8542

Email: customercare@complianceonline.com

Read Frequently Asked Questions

Companies are unsure on what exactly to qualify or re-qualify test and document. The main reason is that unlike for analytical methods there are no clear standards for equipment qualification.

Description

The USP has developed a new standard for analytical instrument qualification (AIQ). It will be official by August 1, 2008.

Why Should You Attend:

Analytical instruments should be qualified to demonstrate suitability for the intended use. Despite the fact that instrument qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify or re-qualify test and document. The main reason is that unlike for analytical methods there are no clear standards for equipment qualification. This is changing. The USP has developed a new standard for analytical instrument qualification (AIQ). It will be official by August 1, 2008. When implemented right the standard also helps to reduce overall qualification costs.

Areas Covered in the seminar:

  • FDA and EU requirements for analytical instrument qualification.
  • Most common inspection problems.
  • Terminology, scope and principles of the new USP chapter.
  • AIQ and its relation to method validation, system suitability testing and quality control checks.
  • Essential steps for AIQ: DQ, IQ, OQ, PQ.
  • Purpose and contents of equipment qualification phases: design qualification, installation qualification, operational qualification, performance qualification.
  • Recommendations for firmware and software validation.
  • Roles and responsibilities: QA, manufacturer, user.
  • Approach for automated systems (incl. firmware/computer systems).
  • Requalification after equipment changes (move, repair, firmware upgrade, hardware upgrade).
  • What documents should be available for the FDA.

For easy implementation, attendees will receive:

  • Copies of all slides
  • SOP: Equipment Qualification
  • SOP: Allocating Analytical Instrument to USP <1058> Categories
  • SOP: Procedures and Deliverables for Qualification of USP <1058> Instrument Categories

Note: These complimentary hand-outs will be sent to customers on request. Please email customercare@complianceonline.com for these documents, stating your order number, and they will be emailed to you within 4 working days.

Who will benefit:

  • Everybody involved in analytical instrument qualification
  • Laboratory Managers
  • QA managers and personnel
  • Analysts
  • Metrology groups
  • Validation specialists
  • Suppliers of analytical equipment
  • Regulatory affairs
  • Training department
  • Consultants

Instructor Profile:

Ludwig Huber, is one of the leading experts on validation and compliance issues for laboratories. He is the worldwide director for FDA Compliance at Agilent Technologies. A frequent speaker at industry gatherings, Dr. Huber was voted the ‘Presenter of the year’ from among 170 experts by more than a 1000 IVT (http://www.ivthome.com/) conference attendees in 2002. Dr. Huber has conducted over a 100 on-line audio/tele/video seminars and is the author of the books “Validation and Qualification in Analytical Laboratories” and "Validation of Computerized Analytical and Networked Systems", Interpharm Press.

ComplianceOnline is a Regulatory Affairs Professionals Society(RAPS) RA Professional Development Portal provider. ComplianceOnline is committed to enhancing the ongoing professional development of regulatory affairs professionals and other stakeholders through appropriate regulatory affairs learning activities and programs ComplianceOnline has agreed to follow RAPS-established operational and educational criteria.. Credit available for Live webinar Attendees only.

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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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