Arslan Arshad

I support pharmaceutical quality, compliance, and regulatory documentation, with experience in hospital pharmacy operations at M.F. Hospital & Research Centre and GMP-focused manufacturing work at Medicross Pvt Ltd.

At Medicross, I performed QC testing and batch-record verification across manufacturing batches, achieving zero batch release deviations during my tenure. I also supported deviation identification, CAPA documentation, SOP compliance, in-process controls, and ALCOA+-aligned record-keeping.

My MSc research at Kingston University examined regulatory considerations for nanomedicine under ICH and EMA frameworks, translating scientific and regulatory data into CTD Module 2-style technical reports. I'm focused on regulatory affairs and quality roles in GCC/SFDA-regulated markets.