Upcoming Live Training Programs by Anthony J. DeStefano, Ph.D. :

FDA Guidance on Analytical Procedures and Method Validation and its Relationship to Upcoming ICH Q2 and USP <1220> Initiatives
Live Training Webinar - Date: Wednesday September 25, 2019 - Time: 10:30 AM - 12:30 PM ET (New York Time)
Instructor: Anthony J. DeStefano Ph.D.
Detailed Information>>>


Elemental Impurities Compliance for the Pharmaceutical Industry; Understanding and Implementing USP General Chapters <232> & <233> and A Review of ICH Q3D
Live Training Webinar - Date: Tuesday October 8, 2019 - Time: 10:30 AM - 12:30 PM ET (New York Time)
Instructor: Anthony J. DeStefano Ph.D.
Detailed Information>>>


2020 Annual Pharmaceutical Impurities Training Program; A Comprehensive Examination of the Key Best Practices and the Latest Regulatory Expectations from FDA, ICH, EMEA and USP

4-Part Live Training Program - Instructors: Kim Huynh-Ba and Anthony J. DeStefano Ph.D.

Part 1: FDA Guideline on Analytical Procedures and Method Validation with Application to Impurities
Live Training Webinar - Date: Wednesday Feb 5, 2020

Part 2: Understanding the Impact of FDA, ICH, USP and EMEA impurity guidelines, and data needed to establish acceptance criteria according to the FDA Manual of Policy and Procedure (MAPP)
Live Training Webinar - Date: Wednesday Feb 19, 2020

Part 3: Elemental Impurities Compliance for the Pharmaceutical Industry; Understanding and Implementing USP General Chapters <232> & <233> and A Review of ICH Q3D
Live Training Webinar - Date: Wednesday Mar 4, 2020

Part 4 : Monitoring Organic Impurities in Pharmaceutical Products to Meet FDA and ICH Q3 A/B Requirements
Live Training Webinar - Wednesday Mar 18, 2020

Detailed 4-Part Live Training Program Agenda>>>