Clinical Trial and Clinical Research Webinars

• Nov 13, Thursday | 01:00 PM EST | 60 Mins

This webinar will show how to convert any ANSI/ASQ Z1.4 (MIL-STD 105) sampling plan into a zero acceptance plan that off...

By WILLIAM LEVINSON

• Oct 24, Friday | 01:00 PM EST | 90 Mins

The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability buil...

By Carolyn Troiano

• Jan 06, Tuesday | 01:00 PM EST | 90 Mins

This course provides guidance on how to perform QC analytical test method validations and transfers. One of the most cri...

By John C. Fetzer

• Oct 15, Wednesday | 01:00 PM EST | 90 Mins

If you work in the GMP regulated industry you not only need to address human error deviations because they are an inconv...

By GINETTE COLLAZO

• Jan 06, Tuesday | 01:00 PM EST | 90 Mins

This course will educate you about various key elements of sterility assurance and contamination control such as Cleanro...

By Kelly Thomas

• Jan 06, Tuesday | 01:00 PM EST | 90 Mins

In the manufacture and quality control of medicinal products, compliance with the GMP rules is the decisive aspect of ma...

By Kelly Thomas

• Jan 06, Tuesday | 01:00 PM EST | 90 Mins

Compliance under GLP can be difficult. The setting up of a system to monitor the performance of methods and instruments...

By John C. Fetzer

• Jan 06, Tuesday | 01:00 PM EST | 90 Mins

The records in a lab – the logbooks for chemicals, reagents, and calibration solutions, sample preparation, instru...

By John C. Fetzer

• Feb 09, Monday | 01:00 PM EST | 90 Mins

Accuracy, the ability of a methodology to give results within acceptable limits when compared to known values, is a fund...

By John C. Fetzer