The Top Method Validation Mistakes – And How to Avoid Them
: 23 Jul 2020
Sector: Clinical, Cosmetic/Personal Care, Food & Beverage, Microbiome, Pharmaceutical
Method validation is legally required to show regulatory authorities that your organization’s method is appropriate for its intended use. If not performed properly, method validation can cause delays in product approval and regulatory problems during commercialization.
Inadequate method validation remains a significant problem during pharmaceutical, biopharmaceutical, and biological product development, approval, and commercial production. The most common mistakes include inadequate method characterization, deficient handling of deviations and discrepancies, inadequate Validation Reports, and not revalidating when necessary. Knowing how to avoid these mistakes will ensure successful validation of analytical methods during Phase III and beyond.
This 90-minute seminar will use the guidance provided by ICH Q2 as a foundation and go beyond to show you how to best prepare and execute your methods validation strategy.
Learn to look out for and avoid common pitfalls including:
The top 10 mistakes people make before starting validation (including inadequate Protocols, failure to formally qualify equipment, deficient robustness studies and more)
- Frequently-seen mistakes made during method validation (including non-compliant handling of Protocol deviations, inadequate oversight of validation done by contract labs, and more)
- Common errors made after method validation work is completed (including deficient Validation Reports, not tracking and trending the method and more)
- In addition, this course will include recent case histories of validation mistakes drawn from FDA Warning Letters and Notices of Deficiency (483s), and how these errors can be avoided. An Annex will be included containing validation deficiencies cited by FDA in the last 5 years.
WHO SHOULD ATTEND
This course will be of benefit to methods development scientists, QC analysts, laboratory managers, validation specialists, QA managers and staff, and anyone involved with regulatory affairs and GMP Laboratory Control Systems compliance.
WHAT TO EXPECT
HOW TO PARTICIPATE
This webinar will be offered live. With your course purchase, you may participate live or view the recording at your convenience (available for 30 days). Access instructions for the live viewing will be emailed to you 3 business days prior to the scheduled date. Access to the recorded version will be available 1 business day after the live course has run.
To access the course, you need only a telephone and computer with internet access.
This webinar is scheduled for live instruction on
Date: July 23, 2020
Time: 1:00 – 2:30 PM EDT
Choose to participate live or listen to the recording afterward!