Advance Your Lab Operation: Minimize Regulatory Risk by Moving to a Customized Instrument Qualification Solution

Changes to Regulatory requirements around Analytical Instrument Qualification (AIQ) have resulted in more responsibility for end-users of instruments to define and implement customized qualification solutions based on their specific User Requirements, Intended Use and Range of Use. Continuing to use Service Vendors "Standard" protocols presents increased Compliance Risk as this will alert Regulatory Inspectors that you are not qualifying your instruments based on your Intended Use.

Presenter: Garry Wright (European Laboratory Compliance Specialist, Agilent Technologies)

Garry Wright is the European Laboratory Compliance Specialist for Agilent Technologies and a member of Agilent's Compliance Council. Garry has over 20 years of experience working in Regulated Pharmaceutical Industry prior to joining Agilent in 2015. During this time he has been involved in the development and implementation of Quality Management Systems (QMS), GxP Training and Auditing. Garry's role within Agilent as a Compliance Specialist is to help develop Agilent products and services from a compliance perspective and assist Agilent customers with compliance challenges they face in their laboratory environments. Garry regularly presents on topics including Regulatory Compliance, Analytical Instrument Qualification and Data Integrity.