Danish Raza Mohd

At Chelmeda Anand Rao Institute of Medical Sciences (CAIMS), I collected patient medication histories and supported clinical case documentation during my Pharm.D clinical training.

I participated in ward rounds and supported medication reviews, drug-interaction checks, and adverse drug reaction monitoring.

Under supervision, I contributed to therapeutic drug monitoring and pharmacotherapy discussions. I also presented clinical cases and participated in patient data collection and therapeutic evaluation.

I've completed a Clinical Research Diploma and an Advanced Diploma in AI for Vigilance / Drug Safety. My training covered ICH-GCP principles, informed consent, clinical trial documentation, CRFs, and pharmacovigilance basics.