Facilities and Equipment is a very broad track intended to challenge those involved in the delivery of pharmaceutical facilities used to support the development, manufacturing, testing, and storage of pharmaceutical industry products meeting quality standards, employing efficient design, project delivery strategies, and adopting sustainable approaches to meet environmental expectations. The 2018 ISPE Annual Meeting & Expo Facilities Equipment Track will include industry owners, industry supplier experts, and innovators ready to share best practices and new approaches to advance efficiencies in the pharmaceutical manufacturing sector.
This year’s topics will address those areas that are currently challenging those who specify, design, and build our manufacturing plants including:
Facilities and Equipment Track session leaders and speakers have put together a program of case studies, industry surveys, practical experience, and forward-thinking strategies. Sessions include:
I look forward to meeting you in Philadelphia this November at the 2018 ISPE Annual Meeting & Expo – come join us as we examine ways to achieve efficiencies in manufacturing.
Through the ISPE Foundation Professional Development Grant program, Silas Tamufor attended the 2023 ISPE Annual Meeting & Expo in October 2023. Tamufor is a PhD student and ISPE Boston Chapter member who began serving as the ISPE Boston Educational Programs Committee Chair in December 2023. He, along with 87 other students and recent graduates, attended the conference thanks to the...
To meet the biopharmaceutical industry’s duty to manufacture safe and effective therapies for patients, a robust quality system is fundamental to success. A quality system should link to quality culture and prioritize focusing on quality, led by management, that fosters sustainable compliance and consistent production of high-quality drugs. Strong quality culture attributes include a proactive...
Stability sampling and testing are key to ensuring that products maintain safety, identity, strength, purity, and quality throughout their claimed shelf life. It is also a regulatory requirement per ICH Q5. However, storing product samples in different environmental conditions, testing those samples for three to five years (or more) after initial manufacture, and properly analyzing and...