Complimentary

These webinars are FREE for anyone to register and attend.  Registered attendees receive access to the webinar for 30 days.  After 30 days, ISPE Members have the benefit of unlimited access to the complimentary webinar recordings and presentations - even if you don't sign up for the webinar. So, if you’re not a Member - Join today!

On
ISPE Member Connect Webinar with Fran Zipp and Tom Hartman As we’re all navigating our way through 2020 and making the most of our virtual interactions, we would like to connect you with the leadership at ISPE through...
On
Resolving & Avoiding Drug Shortages & the Health Crises They Create Webinar Learning Level: Basic Drug shortages are not just a supply chain problem. They are a problem for patients. Sometimes these patients are so at...
On
Learning Level: Basic/Intermediate - Sponsored by: Hold times caused by micro QC test have a significant impact on the manufacturing cycle. Many companies try to overcome this bottle neck by choosing a “continue at risk”...
On
Learning Level: Intermediate - This webinar session is a follow-up to last summer’s popular webinar, “Polishing an Old Gem: Commissioning & Qualification Baseline Guide Update” which gave participants an overview of the...
On
Creating a Vision of the Future – An Evolution or Revolution of the Pharmaceutical Supply Chain Learning Level: Basic In a fireside chat format our speakers will discuss their vision of the Pharmaceutical Supply Chain in...
On
Operational Controls to Mitigate SARS-CoV-2 Challenge to Virus Control Framework in Industrial GMP Manufacturing Facilities Webinar Learning Level: Intermediate - The SARS-CoV-2 worldwide pandemic has presented a...
On
Learning Level: Basic - Implementation of Single-Use Systems (SUS) starts with an effective selection of Single-Use components. This webinar highlights criteria to select and qualify Single-Use components. It expands on...
On
Learning Level: Intermediate - Preparing for full GMP operations requires effective development and deployment of production equipment, procedures, and processes. However, as many experienced leaders can attest, full...
On
Lifecycle Process Validation guidance has been published by FDA in 2011 and by PIC/S and EMA in 2015. This guidance reflects ICH guidance on enhanced development and product quality monitoring practices using approaches...
On
Learn How Implementing Global Best Practices in Asset Management Improves Pharma Operations Topics Covered Pharma Trends and Outlook Discussion History of Asset Management Global Standards Development - PAS 55 to ISO...