I’m a certified pharmaceutical quality control specialist with 10+ years of experience in GMP, GLP, and analytical documentation. I write and review SOPs, methods of analysis, and QC chromatograms aligned with regulatory standards (GMP, ICH, USP). With deep expertise in HPLC/UPLC/GC and audit compliance, I deliver precise, audit-ready documents tailored to your lab or pharma business. Let's ensure your documentation is accurate, professional, and inspection-ready.... Read more