All webinars are scheduled from 11:00AM - 1:00PM EST/EDT

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(In case you missed a topic you can purchase the recording)

2016 Schedule

Jan. 13: A Practical Guide to Excipient Risk Assessments, D. Carter
Feb. 17-18: NSF/IPEC/ANSI 363-2014 GMP Parts 1 and 2, I. Silverstein
Mar. 16: Significant Change, B. Lichtenhan & H. Sturtevant
Apr. 13: Atypical Actives, P. Zawislak
May 4: Elemental Impurities, D. Schoneker
Jun 15: QbD Sampling Guide, B. Carlin & C. Moreton
Sept. 14-15: DMF filing via eCTD, A. Azevedo
Oct. 19: Good Distribution Practices, L. Herzog & P. Malcontento
Nov. 9: Good Supply Practices (GSPs) – Paradigm-Shifting Solutions, Marla Philips
REGISTER! Dec. 14: TEC (Total Excipient Control), D. Schoneker

2017 Schedule

Jan. 18: Validation for Pharmaceutical Excipients, A. Van Meter
Feb 15: US and Canadian DMF Filing via eCTD, A. Azevedo
Mar. 15: Excipients & Nanotechnology, S. Clancy & R. David
Apr. 19: A Practical Guide to Excipient Risk Assessment, D. Carter
May 24-25: Data Integrity for Excipient Makers and Distributors, I. Silverstein
Jun. 14: Additives and "Impurities" in Excipients, J. Zeleznik & G. Collins
Sept. 13-14: Global Regulatory Overview (in conjunction w/AAPS), P. Zawislak
Oct. 11: What Goes In? Excipient DMFs, Technical Files and Registration Documents, M. Raghuram, K. Ulman
Nov. 8: NSF/IPEC/ANSI 363-2014  Overview, I. Silverstein
Dec. 13: TEC Total Excipient Control, D. Schoneker

Price: (Double fees apply for webinars that are scheduled in two parts)

  Member Non-Member Govt. Rate
Single $79 $159 $53
Double $159 $319 $107

*Registration and fee are required for each individual attending from an organization. Any individual who attends the webinar without registering and payment of the fee will be expelled from the webinar.

Webinar Archives

Webinar Archives are available for the following fees:

  Member Non-Member Govt. Rate
Single $75 $150 $50
Double $150 $300 $100

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