iSpeak Blog

Process validation (PV) aims at reassuring a manufacturer of constant product quality. Moreover, it is a regulatory requirement to achieve licensure of a pharmaceutical product Failing to efficiently plan and execute activities here leads to increased time-to-market. Statistics play a pivotal role here, as is shown by the fact that in the 22 pages of the latest FDA guidance document on process...

iSpeak Blog

Wow! You have been with the Society for 40 years! Can you give me a brief summary of your involvement with ISPE and share some of the more interesting experiences and successes you have had with the Society during your lengthy tenure?

iSpeak Blog

Hope everyone is settling into their new reality and staying safe. Your ISPE Annual meeting education organizers have been hard at work setting up a fantastic program to be held in the fall. Check it out on line and plan on joining with colleagues and experts around the world to review and discuss the latest developments in the sector.

iSpeak Blog

The individual stories of patients—and their families—are welcome reminders to the pharmaceutical industry about just how meaningful pharmaceutical development, manufacturing, and delivery are every day to those patients and their families.

iSpeak Blog

When Dave became involved with the pharmaceutical industry in the early 1970’s, pharma engineers had limited resources for guidance when confronted with a problem. Dave joined ISPE in its first year to help the industry develop this type of support. We talked to Dave about his experiences during the past 40 years, and his thoughts about the changes that have been made during that time.

Subscribe to ISPE ISpeak Blogs