Daily Rules, Proposed Rules, and Notices of the Federal Government
This announcement is directed towards professionals involved in the manufacture, control, and regulation of pharmaceutical products who will benefit from these workshops, including process/production engineers, manufacturing personnel, quality assurance/quality control and regulatory affairs professionals, consultants, regulatory investigators, and CGMP compliance officials. Other entities or individuals may also be interested in attending.
We have scheduled four workshops. The locations and times are listed in table 1 of this document.
You can participate in person. Anyone interested in the GMP workshops can register through the contact person (see
Yes, a registration fee is required for this workshop. The registration fee includes workshop reference materials and meals. Registration fees for the Bethesda, MD and Dublin, Ireland workshops are listed in table 2 of this document. The registration fee for both China locations (Beijing and Shanghai) is $550 with no discounts. All fees are given in U.S. dollars.
The notice of participation form, information about the workshops, and other related documents are available from the contact person (see
FDA is cosponsoring these 2-day workshops to provide information and training opportunities for industry as well as CGMP compliance officials.
The workshops will provide information on specific topics designed to educate and guide participants on methodologies and implementation of CGMP as applied to quality drug manufacturing. Presentations by both FDA and industry will provide a regulatory and practical perspective on the current relevant critical topics.