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Complete Guide to GMP in Pharma: From Basics to Advanced

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Monica Sharma

1:56:59

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  • 1 - Introduction.mp4
    00:32
  • 2 - Modules Course Details.mp4
    02:40
  • 3 - What is GMP.mp4
    08:05
  • 4 - GMP Regulation and Practices.mp4
    05:58
  • 5 - GMP Guidelines.mp4
    02:41
  • 6 - Structure and Location.mp4
    08:06
  • 7 - Documentation and Pharma Quality System.mp4
    10:04
  • 8 - FDA 21CFR 210 Guideline.mp4
    13:12
  • 9 - WHO Guideline.mp4
    12:31
  • 10 - CDSCO.mp4
    03:32
  • 11 - Warehouse Quality System.mp4
    07:47
  • 12 - Risk of Not Following GMP.mp4
    03:18
  • 13 - Quality Measures in GMP.mp4
    08:31
  • 14 - Hierarchy in Pharma Industry.mp4
    04:12
  • 15 - QbD Quality by Design.mp4
    10:34
  • 16 - ALCOA and DI.mp4
    08:48
  • 17 - Case Studies.mp4
    06:28
  • Description


    Basics to Advance Compliance Pharma Regulatory Affairs GMP

    What You'll Learn?


    • Understand GMP Fundamentals: Learners will gain a comprehensive understanding of Good Manufacturing Practices (GMP)
    • Regulatory Compliance: Learn to interpret and apply global GMP guidelines like WHO, FDA 21 CFR, and Schedule M for compliance.
    • Quality Control: Implement quality measures and manage risks, including warehouse management and handling non-compliance.
    • Advanced GMP: Master advanced GMP concepts like QbD, ALCOA, and pharma industry hierarchy for maintaining high compliance standards.

    Who is this for?


  • pharma professionals, students and graduates, beginners, regulatory affair professionals, consultant, anyone interested in GMP
  • What You Need to Know?


  • Basic Pharma Knowledge, Interest in GMP, no special tools required, open to all
  • More details


    Description

    Unlock the secrets to pharmaceutical excellence with our comprehensive course on Good Manufacturing Practices (GMP). This course is meticulously designed for professionals, students, and anyone interested in the pharmaceutical industry, covering everything from fundamental concepts to advanced compliance strategies.

    You will explore essential GMP guidelines, Quality by Design (QbD) principles, and key quality measures that are critical to successful pharmaceutical manufacturing. Dive deep into the frameworks of ALCOA (Attributable, Legible, Contemporaneous, Original, Accurate) and Data Integrity, which are vital for maintaining high standards of quality and compliance.

    Through engaging lectures, real-world examples, and practical assignments, you’ll gain the knowledge and skills necessary to ensure product quality, meet regulatory requirements, and prioritize patient safety in the pharmaceutical sector.

    By the end of this course, you will have a thorough understanding of GMP principles and their application in various contexts. This knowledge will empower you to contribute effectively to your organization’s compliance efforts and enhance your professional profile.

    Join us today and elevate your expertise in GMP, paving the way for a successful and rewarding career in the pharmaceutical industry! Take the first step toward becoming a valuable asset in this vital field and make a significant impact on health and safety.

    Who this course is for:

    • pharma professionals, students and graduates, beginners, regulatory affair professionals, consultant, anyone interested in GMP

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    Monica Sharma
    Monica Sharma
    Instructor's Courses
    MS BioAcademy is a platform for imparting quality educational tutorials to all the learners who wish to understand the concepts of Biotechnology, Genetics, Molecular Biology, Biology etc for lifelong learning. These video lectures  are very simple and easy to understand for even non-biology individuals. Its a mission to impart quality knowledge and education to all.
    Students take courses primarily to improve job-related skills.Some courses generate credit toward technical certification. Udemy has made a special effort to attract corporate trainers seeking to create coursework for employees of their company.
    • language english
    • Training sessions 17
    • duration 1:56:59
    • Release Date 2024/12/03