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The Pharma URS Guide: Avoid These Costly Mistakes 📌 What is URS in Pharma? Why is it so important in equipment selection, qualification, and validation? In this video, I dive deep into User Requirement Specification (URS) - a critical document that forms the foundation of GMP-compliant pharmaceutical operations. Whether you're in Quality Assurance (QA), Quality Control (QC), Engineering, IT, or Regulatory Affairs, understanding URS is a must. 🎯 In This Video, You Will Learn: What is a URS in the pharmaceutical industry? Why URS is essential for validation and regulatory audits Who prepares a URS and how it's structured Where URS is used – equipment, software, labs, HVAC, and more Common mistakes in writing URS documents URS in the V-model validation lifecycle Real-world audit examples and tips to avoid compliance issues 📁 I also cover a sample URS format with examples for pharma equipment and GxP systems to help you get started right away. User Requirement Specification in pharma, URS format, URS pharma equipment, URS validation, GxP compliance, pharmaceutical documentation, URS in FDA audit, pharma validation lifecycle, 21 CFR Part 11, GAMP5, URS template, URS pharma example, URS QA QC Engineering ✅ Who Should Watch? This video is ideal for: Pharmacy students QA/QC professionals Pharma engineers Regulatory compliance officers Anyone involved in pharmaceutical validation 📩 Need a URS template? Comment below and I'll send it to you! 🔔 Don't forget to LIKE, SHARE, and SUBSCRIBE to PharmaHealth Insights for more videos on pharma documentation, regulatory updates, and career growth tips! Get all Pharma and Healthcare news, content and tips at: Linkedin: / pharmahealth-insights Facebook: / rajesh19733 Twitter: https://x.com/rajesh19733 Blog: https://rajeshkapoorpharma.blogspot.com WhatsApp: https://whatsapp.com/channel/0029Vavm... #pharma #qualification #urs guide #URS #PharmaValidation #PharmaceuticalIndustry #GMP #QAQC #PharmaTraining #URSFormat #PharmaDocumentation #FDA #URSPharma #URSExplained