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DESCRIPTION:Achieve confidence that your company is GCP inspection ready b
 y walking through every step of the inspection preparation and execution 
 process. Leave having heard directly rom the regulators themselves about 
 inspection trends\, what you need to implement to ensure you are prepared
 \, and understand how technology and effective training can be utilized t
 o drive a culture of quality\, and a continued state of GCP inspection re
 adiness.\n\nTOP REASONS TO ATTEND- Discuss quality culture as the heart o
 f any successful inspection readiness plan- Assess current inspection ris
 ks to provide the building blocks for your GCP inspection readiness plan-
  Utilize mock inspections as a quality tool to focus risk mitigation effo
 rts- Understand the current regulatory environment and the impact on GCP 
 inspections- Harness the power of the Trial Master File (TMF) to drive in
 spection readiness processes- Ensure all stakeholders understand their ro
 le leading up to and during an inspection- Leverage GCP audits to assess 
 the inspection readiness of your clinical vendors and sites- Outline sequ
 ence of events for managing an inspection to understand the different rol
 es- Recognize training as a core component to an effective inspection rea
 diness approach&nbsp\;\n
DTEND:20231206T170000
DTSTAMP:20260307T143226Z
DTSTART:20231204T090000
LOCATION:Online\, Online\, Online\, Online\, Online\, Online\,
SEQUENCE:0
SUMMARY:Achieve confidence that your company is GCP inspection ready by wa
 lking through every step of the inspection preparation and execution proc
 ess. Lea...
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