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FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials

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Event# 16506203915

Event Details

Course Description:

Manufacturing an investigational product for the initial pilot clinical trials could pose a considerable logistical and financial challenge to developers. The first-in-man and pilot clinical trials are usually conducted in very small number of healthy participants with lower doses primarily to establish safety and hence do not need a significant amount of investigational material. The US FDA allows developers to test early stage investigational products under relaxed GMP requirements.

The manufacturing requirements for early stage clinical trials are designed to assure adequate quality of the investigational product being tested without the excessive regulatory burden of full-scale GMP manufacturing. This workshop will present the current regulations, guidance documents and regulatory strategies available for manufacturing an early development stage product for Phase I and first-in-man clinical trials. Also discussed will be logistical issues with managing the supply of an early stage investigational product, and requirements for stability testing, storage and shipping, labeling, and documentations. Perspectives for different classes of products will be presented using case studies.

Event Details:

Date: August 23- August 24, 2012
Time: 08:00 AM-03:30 PM EDT
Cost: $1099 : Seminar One Registration
Group Registrations :Call Toll Free +1-888-717-2436
Registration: SIgn-Up on-line now. Add to your shopping cart.

FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials

Address : Hampton Inn Philadelphia City Center 1301 Race Street Philadelphia PA
Phone : 16506203915   (Always call and confirm events.)
Fax : +1-650-963-2556

Web Address :
Admission Fee : $1099

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