FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials
23rd August 2012 — 24th August 2012

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.

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.

Suggested Attendees

Who will Benefit: * Directors * Managers * Supervisors, and lead workers in Regulatory Affairs * Quality Assurance and Quality Control

Expected Number of Attendees

200-500

View Conference Website: FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials

Price of Attendance

$1,099.00

Brochure

View Event Brochure

Location

Hampton Inn Philadelphia City Center 1301 Race Street
Philadelphi
United States
19107