How to Minimize Compliance Risk in Regulated Laboratories | LabRulez LCMS

How to Minimize Compliance Risk in Regulated Laboratories

ZÁZNAM | Proběhlo Čt, 24.11.2022
Během tohoto webináře se podíváme na některé nejnovější trendy a žhavá témata, která jsou v regulovaných laboratořích sledována.
Agilent Technologies: How to Minimize Compliance Risk in Regulated Laboratories

Agilent Technologies: How to Minimize Compliance Risk in Regulated Laboratories

During this webinar we will take a look at some of the latest trends and hot topics that are being observed within regulated laboratories. We will also discuss various processes that you need to implement in order to remain compliant with the latest regulatory guidance and minimize your inspection risk.

Specific topics that will be covered will include:
  • Custom Analytical Instrument Qualification (AIQ) based on User Requirement Specifications (URS)

  • Repair Qualification (RQ)

  • Hidden costs of Self-Qualification

  • Computer System Validation (CSV)

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

Garry Wright is the European Laboratory Compliance Specialist for Agilent Technologies and a member of the Agilent Compliance Council. Garry worked in Regulated Pharmaceutical industry for 20 years prior to joining Agilent.

His industrial experience focussed on development and implementation of Quality Management Systems, GMP training and Compliance Auditing. Garry’s role within Agilent is to provide Compliance Consulting services to Agilent and our customer network.

Garry has presented topics relating to Regulatory Compliance, Data Integrity and Instrument Qualification at a variety of Compliance forums over the last 7 years since joining Agilent.

Agilent Technologies
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