Altaf Choudhary

Background

About Altaf Choudhary

I am a dedicated Regulatory Affairs professional with hands-on experience in In-Process Quality Assurance (IPQA) within the pharmaceutical manufacturing sector. With a strong understanding of GMP guidelines, regulatory compliance, and quality management systems, I work to ensure that every stage of production meets the highest regulatory standards. My background includes real-time line clearance, in-process checks, deviation handling, and documentation review, ensuring product quality and regulatory adherence at every step. I have collaborated closely with cross-functional teams including Production, Quality Control, and RA to ensure smooth audits and inspection readiness. I am passionate about maintaining product integrity, supporting regulatory submissions, and driving continuous improvement initiatives to exceed compliance expectations. IPQA Monitoring and Line Clearance Regulatory Documentation and Compliance Good Manufacturing Practices (GMP) Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) Review Deviation, Change Control, and CAPA Management Internal Audits and Regulatory Inspections (USFDA, MHRA, WHO) SOP Preparation and Training Risk Assessment and Quality Improvement Initiatives * complete 6 month APCRM (Advance pharmacovigilance certificate and research management) certificate course from clini India