Fact Sheet: Pharmaceutical Packaging Assessment Following USP <1663> and USP <1664> Guidance

Gain practical insights into the key principles for assessing extractables and leachables associated with the assesment of pharmaceutical packaging and delivery systems in accordance with USP <1663> and USP <1664>. Learn what each chapter covers, and the analytical considerations needed to support product quality, patient safety, and regulatory expectations.

Find inside our guide:

• An overview of the key points in USP chapters <1663> and <1664>
• Learn about analytical strategies for pharma packaging assessment
• How these studies support product quality, patient safety, and regulatory submissions

Download our concise guide for an introduction to evaluating pharmaceutical packaging and delivery systems in accordance with USP guidance.