Validation of HPLC/UPLC Methodologies

This training program will cover in detail the key elements of HPLC and UPLC method validation to ensure compliance with FDA GLP and ISO 17025 requirements.

John C. Fetzer | Duration:60 Minutes | Price: $150.00 View Details

15
April
2020
Wednesday

10:00 AM PDT | 01:00 PM EDT

Are You Ready for FDA FSMA Preventive Controls Audit?

This course will examine new FDA authority, introduces examples of Preventative Controls, leading into minimal recommended preparation steps for handling the new FDA FSMA requirements, including managing Form #483, or the FDA Warning for non-compliances.

Gina Reo | Duration:60 Minutes | Price: $150.00 View Details

24
April
2020
Friday

10:00 AM PDT | 01:00 PM EDT

What to Expect with the new FSMA Intentional Adulteration Regulation

IA establishes requirements to prevent or significantly minimize acts intended to cause wide-scale public health harm.

Gina Reo | Duration:60 Minutes | Price: $150.00 View Details

Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Test method validation is an often-confusing requirement for medical devices. A fundamental issue is the role-reversal between the test method and the product or process it is designed to detect.

Speaker: Jose Mora | View Anytime | Duration: 60 Minutes | Price: $190.00 | View Details