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FALLS CHURCH, Va., July 24, 2020 /PRNewswire-PRWeb/ -- Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials **A CenterWatch SOPs Manual** https://www.centerwatch.com/products/category/1065-sops/product/471
One of the impacts of the COVID-19 pandemic is that sponsors no longer see remote monitoring as a nice-to-have option but as a must-have. Many are turning to a risk-based monitoring approach and focusing on the most essential aspects of trials since time and resources are limited.
How should one adapt monitoring plans?
Risk-based monitoring requires processes not normally covered in monitoring SOPs. The newest addition to CenterWatch's library of SOP manuals, Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials, provides readers with the information needed to adapt monitoring plan to changing times.
Gain insights and start using these SOPs, along with templates and worksheets, in one's daily practice and as part of the organization's training program.
Order the manual today to receive essential guidelines:
Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials **A CenterWatch SOPs Manual** https://www.centerwatch.com/products/category/1065-sops/product/471
Price: $1,295
Easy Ways to Order: Online: https://www.centerwatch.com/products/category/1065-sops/product/471 By phone: 888.838.5578 or 703.538.7600
About CenterWatch: Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.
SOURCE CenterWatch
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One of the impacts of the COVID-19 pandemic is that sponsors no longer see remote monitoring as a nice-to-have option but as a must-have. Many are turning to a risk-based monitoring approach and focusing on the most essential aspects of trials since time and resources are limited.
How should one adapt monitoring plans?
Risk-based monitoring requires processes not normally covered in monitoring SOPs. The newest addition to CenterWatch's library of SOP manuals, Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials, provides readers with the information needed to adapt monitoring plan to changing times.
Gain insights and start using these SOPs, along with templates and worksheets, in one's daily practice and as part of the organization's training program.
Order the manual today to receive essential guidelines:
- Identify FDA recommendations for remote monitoring and communication practices
- Determine critical types of data and processes
- Assess risk in a clinical trial
- Evaluate factors to consider when developing a monitoring plan
- Understand the structure and content of risk-based monitoring reports
Standard Operating Procedures for Risk-Based Monitoring of Clinical Trials **A CenterWatch SOPs Manual** https://www.centerwatch.com/products/category/1065-sops/product/471
Price: $1,295
Easy Ways to Order: Online: https://www.centerwatch.com/products/category/1065-sops/product/471 By phone: 888.838.5578 or 703.538.7600
About CenterWatch: Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.
SOURCE CenterWatch
