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How Oncology Biotechs Can Achieve Always Audit Ready Clinical Operations

 
  October 15, 2024  
     
 
Xtalks, Online
2024-11-26


Discover how companies can maintain a constant state of audit-readiness using lean methodologies and strategic tools.

In this webinar, the expert speaker examines how a niche Canadian oncology clinical research organization (CRO) deploys the ‘silver bullet’ that keeps their organization always audit-ready. The speaker will focus on how building a robust team foundation is important, how lean methodologies and tools are effective, how to maintain audit readiness, how collaborators can be integrated in the audit process and how an audit-ready organization should function.

The attendees will also get access to the white paper “Expert Guidance to Key Advantages of Canadian Regulatory Landscape,” which focuses on how to navigate the regulatory landscape.

Register for this webinar today to understand how oncology CROs can help streamline audit processes and ensure continuous compliance with regulatory requirements.

Keywords: Cancer, Good Clinical Practice, Clinical Research, CRO, Oncology, Clinical Operations, Oncology Trials, Oncology Clinical Trials, GCP, Therapeutic Areas, Audit, Sites, GCP Compliance
 
 
Organized by: Xtalks
Invited Speakers: Julie Martin, MSc, Lean Certified, CEO, Scimega
 
Deadline for Abstracts: 2024-11-26
 
Registration: Free Registration
E-mail: tristan@xtalks.com
 
 
   
 
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