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Introduction To Cgmp In Biopharmaceutical Industry - OneDDL - 01-01-2024 Free Download Introduction To Cgmp In Biopharmaceutical Industry Published 1/2024 MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz Language: English | Size: 151.36 MB | Duration: 0h 36m cGMP, Quality by Design (QbD), aseptic processing, biologics What you'll learn Comprehensive Understanding and Practical Application of cGMP Principles Quality by Design and Process validation Levels of Quality Management Systems Control strategies Cleanroom requirements Requirements No previous experience required Description - Are you an engineer or a scientist who wants to break into the emerging biomanufacturing field?- Are you an R&D specialist who wants to know more about the bioprocess development and validation?- Are you working in Market Access or Regulatory Affairs that need to know the language used in cGMP?If you've answered yes to any of these questions, this course is designed for you! I'm Taylor, with an MEng degree in Biomanufacturing from a World Top 30 university and years of experience in the biopharmaceutical industry, I've launched BioMANU, a channel aimed at disseminating essential knowledge about biomanufacturing. I truly believe that by having more professionals access to cutting-edge processes, we can enhance global biologics supply while reducing costs.Biologics are shaping the future of pharmaceuticals, making it crucial for professionals to grasp essential cGMP components. Throughout this 30-minute crash course, you will gain insight into vital concepts of cGMP in biomanufacturing. This includes its distinctions from traditional pharmaceutical practices, the quality by design (QbD) framework, environmental monitoring, aseptic processing, process validation, and more. By mastering cGMP principles, it will not only elevate your work standards but also foster seamless communication and collaboration across diverse teams within the industry.Feel free to explore our demo videos and other courses related to biomanufacturing that we offer. I can't wait to have you join us! Overview Section 1: Introduction Lecture 1 Introduction Lecture 2 Drug Development Process for Biologics Section 2: Module 1: Background Lecture 3 Background of cGMP & Biologics Section 3: Module 2: Quality Management System (QMS) Lecture 4 What is QMS in Biomanufacturing? Lecture 5 QMS Tools You Should Know Section 4: Module 3: GxP in Biopharmaceutical Industry Lecture 6 Product: QbD Part 1-Introduction Lecture 7 Product: QbD Part 2-CPP & CQA Lecture 8 Product: QbD Part 3-Design of Experiment (DoE) Lecture 9 Product: QbD Part 4 - Risk, Validation & PAT Lecture 10 GxP Introduction Lecture 11 Process Part 1: Aseptic Processing Lecture 12 Process Part 2: Good Documentation Practice (GDP) Lecture 13 Premises Lecture 14 Personnel Lecture 15 Conclusion This course is designed for individuals aspiring to or currently engaged in the biopharmaceutical industry, seeking a comprehensive understanding of Current Good Manufacturing Practice (cGMP) and its application in ensuring product quality and compliance. Homepage [To see links please register or login] Recommend Download Link Hight Speed | Please Say Thanks Keep Topic Live [To see links please register or login] No Password - Links are Interchangeable