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The human factors team at Veranex has reviewed the NMPA Guidance Draft 01 and Draft 02 and submitted feedback to the agency. We’re committed to helping you stay informed about the latest updates and clarifications in the ever-evolving regulatory...
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Introduction Nanomaterials, tiny scientific wonders that are invisible to the naked eye, hold the potential to revolutionize numerous facets of our...
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What are some of the challenges with database builds for medical device studies, given the current regulatory requirements? What are the important...
5 min read
The landscape of modern healthcare has been completely transformed by the development of cutting-edge medical devices. From life-saving implants to...
Automation in clinical data management (CDM) is becoming increasingly popular due to the increasing volume and complexity of data being generated by...
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The 19th Precision in Clinical Trials (PCT) Summit – Amsterdam brought together a wide range of representatives from the life sciences industry, from...
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Susanah and Tucker, A Mother-Son Duo In 2016, Susannah Ashcroft drove home from an appointment at St. David’s Center for Child and Family Development...
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Vigilance reporting and postmarket surveillance of medical devices are among the many requirements documented in the EU MDR (2017/745) to ensure the...
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A team from Veranex Data Management & Analytics recently traveled to Hyderabad, the capital of the Indian state of Telengana, for BioAsia 2023....
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In this installment of our “Meet the Team” blog series, we talk to Danita Harris, Senior Vice President and General Manager of Data Management and...
