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Excipient GMP Compliance in Person Workshop



September 18 - 20, 2024
IPEC-Americas Headquarters
3138 10th Street N., Suite 300
Arlington, Virginia

To register for this event add it to your cart. You will be prompted to create an account to complete your purchase.

Save When You Bring Your Team
Register your staff using the same email domain to take advantage of our "Buy 5 get 1 Free" offer and 10% off each additional attendee after the 6th. For more information contact ipecamer@ipecamericas.org.

Workshop Overview:
Compliance with excipient GMP/GDP is important to everyone (not just auditors) involved in the manufacture, distribution or use of excipients. This workshop includes analyzing essential elements and expectations related to excipient good manufacturing practice and good distribution practices for materials intended for use in pharmaceuticals or dietary supplements. This workshop reviews the EXCiPACT Excipient GMP Certification scheme and the requirements of the updated NSF/IPEC/ANSI 363-2019.

After completing this hands-on, interactive workshop
> Participants will be able to plan, conduct and document an audit of excipient manufacturing facilities for conformance to excipient GMP expectations.
> Excipient makers will be able to assess their conformance to industry standards and guides such as NSF/IPEC/ANSI 363, EXCiPACT and the IPEC PQG GMP Guide, and remediate any gaps.
> Excipient users will be able to assess their suppliers for adequate conformance to industry standards and guides including the EU Falsified Medicines Directive (FMD) Guideline for determining GMP for excipients.
> Participants will be able to identify and remediate deficiencies in data integrity.

This workshop is the best place to
> Identify compliance expectations for excipient GMP/GDP
> Learn how to assess improvement needs at your own or your suppliers' facilities
> Learn how to ready your facility audit or certification audit
> Update your audit report-writing skills
> Learn how to develop reports to management to support GMP/GDP compliance
> Understand the current issues concerning the manufacture, distribution and use of excipients as identified by IPEC

Schedule of Sessions
Wednesday, Sept 18 - 8:30am-4:30pm ET
Thursday, Sept 19 - 8:30am-4:30pm ET
Friday, Sept 20 - 8:30am-4:30pm ET

This workshop will be in person and will be hosted at our Arlington, Virginia headquarters.

A mock-audit session is scheduled for Friday morning Sept 20, which is a highlight of the workshop. Please keep this in mind you will not want to miss this important hands-on activity! Discussion and findings about the mock audit session will take place Friday afternoon.

A copy of the NSF/IPEC/ANSI - 363 standard is available for purchase from either the NSF or ANSI web sites for a fee of $195. The standard is not provided to course participants.

Click here for a list of local hotels: Local Area Hotels

Please do not hesitate to contact us if you have any questions at all,

IPEC-Americas Staff
ipecamer@ipecamericas.org
571-814-3449

Cancellation Policy-Workshops

Must be made in writing and can be mailed or e-mailed to:

IPEC-Americas Workshops
3138 10th Street
Arlington, VA 22201
Suite 500
E-mail: ipecamer@ipecamericas.org

Registration fees (less 5% non-refundable service fee) are refundable if cancellation is received at least three weeks (21 calendar days) prior to workshop start date (less service fees). Cancellations received thereafter are non-refundable. Registrations are transferable to other company representatives if requested via mail or e-mail up to 5 business days before the workshop.

IPEC-AMERICAS IS NOT RESPONSIBLE FOR ANY TRAVEL EXPENSES OR FEES INCURRED BY PARTICIPANTS.