"Reviewed and approved by the AIChE Education Services Committee 2005"

WHAT YOU WILL LEARN

• Overview the entire drug development process from laboratory to the marketplace.
• Gain a clear understanding of the unique integration of research and development, manufacturing, quality assurance, and regulatory affairs in the launching of a new drug.
• Examine various concepts unique to the pharmaceutical industry, including those involving scale-up, technology transfer, and the operability envelope.

WHO SHOULD ATTEND

You require an integrated look at the technical, regulatory, and other key aspects of bringing a new drug to market.

This course is recommended for research chemists and engineers, production supervisors, analytical chemists, R&D managers, material managers, process engineers, and QA and DRA professionals.