This is an expansion of the “Blockchain for Pharmaceutical Engineers” article in the Jan-Feb 2019 edition of Pharmaceutical Engineering® magazine. The first part of the webinar will provide an introduction into the...
One Size Does Not Fit All: Strategies for Bringing Advanced Therapy Medicinal Products to Market The number of advanced therapy medicinal products (ATMP) on the global market is fewer than expected despite the large...
Learn how data science can be beneficial for successful tech transfer from development to commercial and from site to site. The speakers will share tips on designing robustness to identify NORs and PARs for platform...
The ISPE Baseline Guide® Water and Steam Systems (Third Edition) aims to assist with the design, construction, operation, and lifecycle management of new and existing water and steam systems. It is intended to help meet...
On- and in-line analysers are used in the framework of PAT (Process Analytical Technology) for controlling and monitoring unit operations in pharmaceutical operations for both batch and continuous manufacturing. The most...
The introduction of advanced automation and the increasing interconnectivity of Industry 4.0 is not only revolutionizing the Pharma industry but also introducing many new challenges and production roadblocks. Understand...
Recordings of Past Webinars ISPE Members have the benefit of unlimited access to the webinar recordings 30 days after the live webinar. Each webinar will feature leading subject matter experts covering critical, relevant...
This webinar will introduce the revision to the ISPE Baseline Guide Vol 5: Commissioning and Qualification. The guide was first issued in 2001 and reflective of that time. With emerging markets, changes in the regulatory...
This webinar provides an overview of new and forthcoming ISPE GAMP® Data Integrity guidance and real-world experiences on applying data integrity in the field. The speakers will address the following topics: Overview of...
This webinar will discuss the lifecycle of computerized laboratory equipment, with some discussion of the similarities and differences to computer system validation, and the use of quality risk management to right-size...
