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Inside IPEC

Inside IPEC–Americas: Evaluating Excipient Stability

September 2, 2009
By:Philip H. Merrell, Irwin Silverstein, PhD
Pharmaceutical Technology

IPEC's new stability testing guide takes into account the full supply chain's storage conditions.

Good Distribution Practices for Pharmaceutical Excipients

May 2, 2009
By:Mathias Brenken, Andreas Lekebusch, Wilhelm Gierling, Steve Hewitt, Allan Whiston, Frank Milek
Pharmaceutical Technology

The GDP committee of IPEC–Europe is trying to seal one more broken link in the supply chain. This article contains bonus online-exclusive material.

Regulation for Excipients is Brewing Across the Atlantic

February 2, 2009
By:Phil Taylor
Pharmaceutical Technology

Without any GMP guidelines for excipients in Europe, change can't come soon enough for some industry groups.

IPEC's New Safety Evaluation Procedure: A Q&A with IPEC Chairman Dave Schoneker

November 2, 2008
By:Maribel Rios
Pharmaceutical Technology

IPEC Chairman Dave Schoneker discusses current efforts toward facilitating regulatory reviews of new excipients.

Dual-Use Labeling

July 2, 2008
By:William D. Carter
Pharmaceutical Technology

Clear labels for substances that can be used as excipients, APIs, or both are critical to end-product use.

Inside IPEC–Americas: Excipient Audits and API Audits are Worlds Apart

May 2, 2008
By:Irwin Silverstein, PhD
Pharmaceutical Technology

The less complex nature of excipient manufacturers, as compared with API manufactures, carries many benefits.

Inside IPEC-EUROPE: Pharmaceutical Excipients—The View from the EU

April 2, 2008
By:Phil Taylor
Pharmaceutical Technology

A changing regulatory environment is on the horizon for excipient suppliers and users.

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