2024 - How Oncology Biotechs Can Achieve Always Audit Ready Clinical Operations
Date2024-11-26
Deadline2024-11-26
VenueONLINE-VIRTUAL, USA - United States
KeywordsLife Sciences; Clinical Trials; Pharmaceutical Regulation
Topics/Call fo Papers
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
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
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- Moneyball for Drug Development: How Causal Inference can Increase the Probability of Success in Clinical Trials
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- Leveraging EMR Data and Patient Engagement to Maximize Clinical Trial Recruitment
Last modified: 2024-10-16 04:55:03