It’s time for another edition of Reading Roundup featuring the top blog posts of September 2017. Start off your week by catching up on what the pharmaceutical industry was reading in September.
5 Key Steps in the Calibration Optimization Journey
John Cummins, CPIP, Managing Director of Specialist Calibration Company, Cal OpEx has over 13 years' experience in the pharmaceutical and bio-pharmaceutical industry. He talked us through the 5 Key Steps needed to begin your Calibration Optimization Journey.
Q&A with Rebecca Brewer: Cleaning Validation Principles
“Cleaning and cleaning validation are of crucial importance to patient safety. Only by ensuring that our processing? equipment is clean through a reproducible process can we have assurance that we do not have product to product, or batch to batch, cross-contamination.” Learn more about what Rebecca had to say about cleaning validation principles.
Q&A with Gary Zoccolante: Pharmaceutical Water
Learn from Gary Zoccolante, Technical Director of Plymouth Rock Water Consultants, on common issues with water systems and how to maintain readiness.
Pay it Forward – Women in Pharma Series
A core mission of Women in Pharma is paying it forward. Here how a mentor impacted one woman’s her career both professionally and personally.
Meeting Unique Requirements for Facility Design and Production
As the 2017 ISPE Annual Meeting & Expo approaches, the program committee members behind the Facilities and Equipment educational track have selected and organized a series of highly technical sessions emphasizing practices and approaches to solve and/or improve the design, construction, maintenance, and management of biopharmaceutical installations. Learn more about the Facilities and Equipment educational track and how you can participate.
The following blog post was provided by Peyton Myers, an undergraduate student at Appalachian State University. Myers attended the 2023 ISPE Annual Meeting & Expo in Las Vegas as an ISPE Foundation Professional Development Grant recipient.
The integration of data science in biopharmaceutical manufacturing, emphasizing data quality, tech transfer efficiency, and process optimization, is the heart of this track. Led by industry experts, discussions explore leveraging digital twins, predictive analytics, and continuous improvement initiatives. Additionally, interactive roundtable discussions provide attendees with a dynamic forum...
The pharmaceutical sector stands at a crossroads of immense possibilities. We are witnessing an unprecedented surge in innovation, fueled by a remarkable partnership between industry and regulatory authorities. For example, there are initiatives fostered by the US Food and Drug Administration (US FDA) to promote innovation with programs such as CATT (CBER Advanced Technologies Team) and ETP...
