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Category: Clinical Trial Management
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Our Solution to the Business Process Management Tool Needed to Maximize the Use of a Safety Database
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![Explore the implications Brexit could have on pharmaceutical regulation and steps you should be taking now to maintain clinical trial business continuity.](https://www.ppd.com/wp-content/uploads/2020/09/BREXIT_shutterstock_623833832_resized-5f60ee8195b1d-380x220.jpg)
![Explore the implications Brexit could have on pharmaceutical regulation and steps you should be taking now to maintain clinical trial business continuity.](https://www.ppd.com/wp-content/uploads/2020/09/BREXIT_shutterstock_623833832_resized-5f60ee8195b1d-150x150.jpg)
Understanding New Pharmaceutical Regulation as We Countdown to Brexit
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Enhancing Communication Between Clinical Trial Sites and the Central Lab During a Global Pandemic
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Moderna Announces Phase 3 COVE Study of mRNA Vaccine Against COVID-19 (mRNA-1273) Begins
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The Top Seven Things to Understand About Data Monitoring Committees
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Regulatory Insights: Focus on China — New Provisions for Drug Registration in 2020
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The Future of Clinical Research: Digitally Transforming What’s Possible
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![FSP Regulatory Affairs: Mitigating COVID-19’s Impact on Clinical Trials](https://www.ppd.com/wp-content/uploads/2020/05/FSP-Regulatory-BlogPost-May2020-shutterstock_1703634364-380x220.jpg)
![FSP Regulatory Affairs: Mitigating COVID-19’s Impact on Clinical Trials](https://www.ppd.com/wp-content/uploads/2020/05/FSP-Regulatory-BlogPost-May2020-shutterstock_1703634364-150x150.jpg)
Regulatory Affairs: Mitigating COVID-19’s Impact on Clinical Trials
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Cell and Gene Therapy Lesson 5: Lab Concierge – Extreme Focus on the Rare Disease Patient and Precious Study Sample Logistics Through an Innovative Lab Concierge Program
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