News|Videos|September 10, 2024

Editorial Advisory Board Spotlight: Susan J. Schniepp

Author(s)Susan Haigney

Susan J. Schniepp, member of the editorial advisory boards for Pharmaceutical Technology, Pharmaceutical Technology Europe, and BioPharm International, provides an update on her experience working in the pharmaceutical industry and what she sees for the industry’s future.

The PharmTech Group’s Editorial Advisory Boards (EABs) provide our editors with expert insights into the development, manufacturing, and quality issues impacting the bio/pharmaceutical industry. EAB members offer valuable input to our editors by reviewing editorial submissions and advising on relevant topics for the magazines and our websites.

This Editorial Advisory Board Spotlight features Susan J. Schniepp, distinguished fellow at Regulatory Compliance Associates, a Nelson Labs company. Susan has been a member of the EAB for several years and a regular contributor to our Ask the Expert print and video series. Susan has offered thought leadership and expert insight into quality and regulatory concerns for our publications. She has also served as the past-chair of the Parenteral Drug Association and was previously a chair with the US Pharmacopeia.

Click the video above to learn more about Susan and her views on the industry.

Click here to access the Ask the Expert series.

Related to this article

PharmTech Weekly Roundup—October 2, 2026
This week on PharmTech, Merck diversified its pipeline, USP emphasizes supply chain security, AI systems are examined, and speakers preview their presentations at CPHI Milan and AAPS PharmSci 360.
CPHI Milan 2026: Nitrosamine Risk Mitigation, Part 1
Capsugel's Bram Baert and Sandrine Picco argue that chasing zero nitrite in pharmaceutical excipients is often impractical and costly. They recommend setting scientifically justified, risk-based limits and consistently staying below them.
Regulatory Roundup—September 2026
The FDA opened an expedited IND pilot, tightened scrutiny of foreign trial data, and finalized a rule recognizing non-animal testing methods. In Europe, the EMA advanced pharmaceutical legislation reform, restricted 2 legacy products, and opened an injectable-iron safety review.