As part of the planning committee, I’m very pleased to share this year’s theme for the 2018 ISPE Quality Manufacturing Conference, June 4-6 in Arlington, VA: Manufacturing and Quality: Present and Future Opportunities to Ensure Continuous Improvement; and we have put together three very interesting and timely tracks on Regulatory, Quality and Manufacturing, and Facilities and Equipment topics.
One session that I am very excited about is the one centered on Contamination Control Strategies. The session will include perspectives from experts in the pharma industry and the U.S. FDA; and will delve into Contamination Control Strategies for sterile and non-sterile manufacturers as an essential consideration for preventing product contamination. Pharma industry experts will share successful ways to communicate and manage contamination controls, with real-life examples.
Attendees will also have a chance to participate in a Q&A session that poses questions such as:
I am really looking forward to attending this session as part of the 2018 ISPE Quality Manufacturing Conference and hope that you will join me in June.
Best Regards
The ISPE Quality Manufacturing Conference is the foremost pharmaceutical quality event of the year. It provides a unique forum for attendees and speakers from industry, academia, and regulatory to address areas for opportunities to assure innovation and continuous supply of high-quality products to our patients.
Here’s what you can expect:
Register by Monday, 26 March to take advantage of our lowest rates — saving you $400 or more!
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...