Reading Roundup: Top Blog Posts from July 2017

It’s time for another edition of Reading Roundup featuring the top blog posts of July 2017. Start off your week by catching up on what the pharmaceutical industry was reading in July.

Standardized Extractables Testing Protocol for Single-Use Systems Biomanufacturing-Part 1

This article from the November-December 2014 issue of Pharmaceutical Engineering® magazine presents a consensus standardized extractables protocol for single-use systems in biomanufacturing. Learn more about how companies are generating SUS extractables testing methods by interpreting regulatory requirements from existing container closure testing methods.

Greatest Failures-Women in Pharma Series

During the Women in Pharma (WIP) breakfast on day two of the 2017 ISPE/FDA/PQRI Quality Manufacturing Conference, 100 attendees gathered for a panel on “Bringing Education to Gender Parity”. Find out what women in the industry had to say as they exchanged their advice and experiences dealing with failure.

New! Decommissioning of Pharma Equipment and Facilities Guide

On 15 June, ISPE announced the release of their latest publication, ISPE Good Practice Guide: Decommissioning of Pharmaceutical Equipment and Facilities. Check out this guide to learn more about the decommissioning and disposing of assets ranging from a single system to an entire facility.

Facility & Life Cycle Quality Management Workshop Recap

Jim McGlade, Science Client Leader for BHDP Architecture, led the “Proactive Approaches to Facility and Lifecycle Quality Management” Workshop at the ISPE/FDA/PQRI Quality Manufacturing Conference. Find out what he, along with three other experts, had to consider on data integrity, quality systems, and process equipment validation and verification.