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)

Webinar Topic Date Presenter
A Practical Guide to Excipient Risk Assessments 13-Jan-16 D. Carter
NSF/IPEC/ANSI 363-2014 GMP Parts 1 and 2 17-Feb-16
I. Silverstein
Significant Change 16-Mar-16 B. Lichtenhan
H. Sturtevant
Atypical Actives 13-Apr-16 P. Zawislak
Elemental Impurities 4-May-16 D. Schoneker
QbD Sampling Guide - Free session 15-Jun-16 B. Carlin
C. Moreton
Global Excipient Regulatory Overview Aug (TBD) M. Raghuram
K. Ulman
DMF filing via eCTD 14-Sept-16
A. Azevedo
3rd Party Audits 19-Oct-16 S. Goode
Good Distribution Practices 9-Nov-16 L. Herzog
P. Malcontento
TEC (Total Excipient Control) 14-Dec-16 D. Schoneker

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

  Member Non-Member
Single $79 $159
Double $159 $319

*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
Single $75 $150
Double $150 $300

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