--- title: Is Your Organization Pharmacovigilance Ready? description: The right strategy to continually evaluate product safety in your clinical trials, through regulatory review is complex. Are you PV ready? image: https://blog.ubc.com/hubfs/PV%20Checklist%20Featured%20Image.png --- [![UBC](https://blog.ubc.com/hs-fs/hubfs/raw_assets/public/UBC_December2021/images/logo-white.png?width=175&name=logo-white.png "UBC")](https://ubc.com/) - [Home](https://ubc.com/) - Services - [Full-Service Clinical Development](https://ubc.com/global-services/) - [Clinical Trial Management & Late Stage Research](https://ubc.com/global-services/trials-and-research/) - [Decentralized Studies & Virtual Engagement](https://ubc.com/global-services/decentralized/) - [Patient & Physician Services](https://ubc.com/global-services/pps/) - [Pharmacovigilance](https://ubc.com/global-services/pharmacovigilance/) - [Risk Management Plans](https://ubc.com/global-services/risk-management/) - [Risk Evaluation and Mitigation Strategies (REMS)](https://ubc.com/global-services/rems/) - 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[Mosaic Technology Platform](https://ubc.com/technology/mosaic-technology-platform/) - [Patient Engagement](https://ubc.com/technology/engage/) - [Think Tank](https://blog.ubc.com/blog) - About - [About UBC](https://ubc.com/about/) - [Awards](https://ubc.com/about/awards/) - [Leadership Team](https://ubc.com/about/leadership/) - [Press Releases](https://ubc.com/about/press/) - [Careers](https://ubc.com/careers/) - [Submit RFI/RFP](https://ubc.com/contact/) Anesthesiology 1. [Home](https://ubc.com/) 2. [Blog](https://blog.ubc.com/blog) 3. Is Your Organization Pharmacovigilance Ready? # Is Your Organization Pharmacovigilance Ready? *Monday, August 17, 2020* ### ![PV readiness checklist](https://blog.ubc.com/hs-fs/hubfs/Imported_Blog_Media/PV-Checklist-Landing-Page-Header-4-1024x551.png?width=500&height=269&name=PV-Checklist-Landing-Page-Header-4-1024x551.png) # **The right strategy to continually evaluate product safety in your clinical trials, through regulatory review and entering the post-marketing setting, is complex. Are you PV ready?** Expectations of global regulators are increasing regarding ongoing, long-term safety assessments, signal detection, and refinement. The [right strategy](https://ubc.com/global-services/pharmacovigilance/) to continually evaluate product safety in your clinical trials, through regulatory review and entering the post-marketing setting is complex. Local market regulations are ever-changing. Technologies to intake, track, and manage workflow are getting more sophisticated. Download our Global Pharmacovigilance Readiness Checklist to guide internal conversations around your organization’s safety strategies: - Safety Systems - Data Migration - Global Case Processing - Regulatory Reporting - Period Reporting - Products to Enhance Operational Delivery - Signal Management & more Complete the form below to receive your complimentary copy of the checklist ## Related Articles ## [Postmarketing Research: Ten Reasons to Plan Early](https://blog.ubc.com/blog/ten-reasons-to-plan-early-and-conduct-postmarketing-research) Manufacturers of biopharmaceutical products and medical devices understand that the regulatory approval of... [Read More](https://blog.ubc.com/blog/ten-reasons-to-plan-early-and-conduct-postmarketing-research) ## [Technology Considerations for Evidence Generation](https://blog.ubc.com/blog/tech-considerations-rwe) {% video\_player "embed\_player" overrideable=False, type='hsvideo2', hide\_playlist=True, viral\_sharing=False,... [Read More](https://blog.ubc.com/blog/tech-considerations-rwe) ## [Data Considerations for Evidence Generation](https://blog.ubc.com/blog/data-considerations-rwe) {% video\_player "embed\_player" overrideable=False, type='hsvideo2', hide\_playlist=True, viral\_sharing=False,... 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