ComplianceOnline

How to Use excel spreadsheet for GXP data and reduce validation cost and time.

This FDA validation training will describe methods for planning and executing spreadsheet validations that satisfy FDA requirements.

Attend this webinar to understand the process of a letter of credit and how to comply with letter of credit requirements to help reduce or prevent costly discrepancies.

In this Food safety training learn about Food preservation, traditional heat treatment, emerging food processing technologies, sterilization, shelf stable products, low acid foods, US FDA and USDA regulations

This Deviation, Investigation and CAPA training will provide valuable assistance on how to avoid costly regulatory action from agencies when they inspect your facilities in pharmaceutical and biotech industries

This Clinical trial auditing training will provide valuable assistance how to conduct clinical trials both using internal resources and also those that outsource the function to CRO’s in pharmaceutical and biotech industries.

With a new emphasis on risk management, regulators expect you to have a robust system. Can your system stand up to scrutiny or will it wilt when exposed to bright light?

It will focus on important microbial issues with pharmaceutical water systems and provide proven solutions for microbial control. Attendees will learn effective sanitation and validation approaches to successfully control biofilm in water systems.

This webinar will help you understand the current quality and regulatory paradigm by comparing and analyzing ICH-Q10 Pharmaceutical Quality System and the FDA’s Quality Systems Approach (FQSA) to Pharmaceutical GMPs .

This training on FTC’s New Substantiation Standards will provide an comprehensive understanding of the new standards, when they will apply and how you can satisfy them.