#SafetyReporting
New York is taking a bold step in AI regulation, requiring frontier developers to register by November and comply with strict safety standards starting in January!

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#NY #CitizenPortal #SafetyReporting #DigitalInnovation #NewYorkAIDevelopers #TransparencyStandards
New York details implementation timeline for RAISE Act, mandates registration and 72‑hour reporting
Governor Kathy Hochul announced a schedule for putting the RAISE Act into operation: frontier AI developers will be asked to register in November and must meet transparency and safety-reporting requirements when the law’s effective date arrives in January.
citizenportal.ai
September 25, 2026 at 3:14 AM
September 27, 2025 at 4:30 PM
Safety Reporting and Pharmacovigilance in Clinical Trials: A Complete Guide
Watch the tutorial here ➡️ youtu.be/G_Hktp4dS-A

#GCP #GoodClinicalPractice #GCPTraining #ICHGCP #MedicalAffairs #ClinicalTrials #SkyHealthAcademy
August 30, 2025 at 8:31 AM
August 29, 2025 at 10:08 AM
Could missing one adverse event cost lives and halt your trial?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 2:31 PM
How fast should you report a life-threatening reaction—24 hours, 7 days, or 15?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 1:15 PM
Are you confident you’d recognize an unexpected serious adverse reaction?

Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
Safety Reporting and Pharmacovigilance in Clinical Trials: A Complete Guide
Understand Safety Reporting and Pharmacovigilance in Clinical Trials—from AEs, SAEs, and SUSARs to DSMBs, timelines, and reporting responsibilities. Essential for Medical Affairs and investigators. In this tutorial, you’ll learn: ✅ What qualifies as an Adverse Event (AE) vs Serious Adverse Event (SAE) ✅ How and when to report SUSARs ✅ The different safety reporting roles for Investigators and Sponsors ✅ Safety Reporting Timelines and Regulatory Expectations ✅ The role of Data Safety Monitoring Boards (DSMBs) ✅ Real-world implications of failing to report properly Whether you’re in Medical Affairs, Clinical Operations, or serving as an Investigator—this tutorial offers a clear, concise breakdown of what’s required to stay compliant and protect patients. 📌 Watch now and enhance your clinical trial safety skills. 👉 Subscribe for more free tutorials: [Insert Channel Link] 👉 More Clinical Research Training: [Insert Playlist Link] 👉 Visit our website for certifications & resources: https://www.skyhealthacademy.net #SafetyReporting #Pharmacovigilance #ClinicalTrials #MedicalAffairs...
youtu.be
August 27, 2025 at 11:10 AM
What does the Data Safety Monitoring Board see before anyone else?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 10:07 AM
Why is every headache, rash, or lab shift vital data?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 8:31 AM
Do you know the difference between a serious adverse event and a SUSAR?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 6:01 AM
Who holds the power to stop your clinical trial—the investigator or the sponsor?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
August 27, 2025 at 4:31 AM
What happens when safety reporting fails—paperwork delays or patient risk?
Watch the tutorial here: youtu.be/G_Hktp4dS-A

#SafetyReporting #ClinicalTrials #GCPref="/hashtag/GCPTraining" class="hover:underline text-blue-600 dark:text-sky-400 no-card-link">#GCPTraining #GCP #ICHGCP #SkyHealthAcademy
Safety Reporting and Pharmacovigilance in Clinical Trials: A Complete Guide
Understand Safety Reporting and Pharmacovigilance in Clinical Trials—from AEs, SAEs, and SUSARs to DSMBs, timelines, and reporting responsibilities. Essential for Medical Affairs and investigators. In this tutorial, you’ll learn: ✅ What qualifies as an Adverse Event (AE) vs Serious Adverse Event (SAE) ✅ How and when to report SUSARs ✅ The different safety reporting roles for Investigators and Sponsors ✅ Safety Reporting Timelines and Regulatory Expectations ✅ The role of Data Safety Monitoring Boards (DSMBs) ✅ Real-world implications of failing to report properly Whether you’re in Medical Affairs, Clinical Operations, or serving as an Investigator—this tutorial offers a clear, concise breakdown of what’s required to stay compliant and protect patients. 📌 Watch now and enhance your clinical trial safety skills. 👉 Subscribe for more free tutorials: [Insert Channel Link] 👉 More Clinical Research Training: [Insert Playlist Link] 👉 Visit our website for certifications & resources: https://www.skyhealthacademy.net #SafetyReporting #Pharmacovigilance #ClinicalTrials #MedicalAffairs...
youtu.be
August 27, 2025 at 2:15 AM
August 26, 2025 at 10:05 PM