All FDA Regulated Industry Webinars

• Oct 29, Wednesday | 01:00 AM EST | 60 Mins

Standard Operating Procedures (SOPs) are the backbone of Good Practice (GxP) compliance in the pharmaceutical, biotechno...

By MATT PEPLOWSKI

• Oct 15, Wednesday | 12:00 PM EST | 60 Mins

Using Process Mapping in Data Integrity Governance.1. Demonstration of key issues 483s and Warning Letter Trend in Data...

By GAURAV WALIA

• Oct 30, Thursday | 01:00 PM EST | 90 Mins

Training programs have evolved. Human reliability or human error is usually attributed to training effectiveness or trai...

By GINETTE COLLAZO

• Nov 20, Thursday | 01:00 PM EST | 90 Mins

Data integrity refers to the accuracy, completeness, and consistency of data over its entire lifecycle. Data integrity i...

By GINETTE COLLAZO

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikel...

By GINETTE COLLAZO

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

Pharmaceutical manufacturing sites continuously compete, even within the same company to maintain production volumes and...

By GINETTE COLLAZO

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

Pharmaceutical manufacturing sites continuously compete, even within the same company to maintain production volumes and...

By GINETTE COLLAZO

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

This webinar describe, As part of the Case for Quality program US FDA noted how an excessive focus by the industry on co...

By Kelly Thomas

• Jan 01, Thursday | 01:00 PM EST | 90 Mins

Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikel...

By GINETTE COLLAZO