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Understanding Adverse Events (AE) vs. Serious Adverse Events (SAE) in Clinical Research
To ensure your safety, we follow the strict guidelines set by the Food and Drug Administration (FDA) and the International Council for Harmonization (ICH). These organizations set the global standard for how we define and report health changes in research.
Mar 134 min read


Why "Doing Okay" is Exactly What Science Needs
Khutaija Noor, MBBS, FCR If you are looking into a clinical trial for a condition like depression, the paperwork can feel like a riddle. The researchers say they need people who are currently struggling with symptoms, but then they ask: " Is your heart healthy? Are your kidneys working well? Have you stayed out of the hospital lately? " It feels like a contradiction. You might think, " I’m here because I’m not okay- so why do I need to be 'stable' in everything else ?" After
Jan 83 min read


Spotlight on Success: Our Lead Coordinator Featured in STAT10
We are thrilled to congratulate our Lead Coordinator, Khutaija Noor, MBBS, FCR , on her recent publication in STAT's First Opinion column! Her insights were featured in an important article discussing the evolving landscape of psychiatric drug development and emerging novel therapies. We’re proud to have her on the Amicis team and excited to see her continue to succeed! Please take a moment to check out her published work: https://www.statnews.com/2025/11/14/psychiatric-drug-
Dec 9, 20251 min read
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