USA | New FDA Guidance on the Content of Human Factors (Usability) Information in Medical Device Marketing Submissions
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UK | HRA Supporting Developers to Access Data and Get the Right Approvals
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UK | HRA Streamlining Applications to Access Data
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CHINA | Revised ICF Template Available on the Chinese Clinical Trial Registry
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CANADA | CADTH (HTA Agency) Publishes RWE and RWD Guidance
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SWITZERLAND | New Federal Act on Data Protection (nFADP)
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USA | FDA RFI for Literature and Survey Study on Brain Computer-Interface Focused Research in Patients with ALS
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USA | FDA Launches Pilot Program to Support Rare Disease Drug Development
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USA | FDA Publishes Final Guidance on Procedures for Handling Post-Approval Studies Imposed by PMA Order
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