Skip to content
Skillpad_Logo

Founded in 1998 in Dublin, Ireland, Skillpad's team of industry-experienced Subject Matter Experts and Consultants believes Pharma, Biopharma, and Life Science Industry manufacturing companies can achieve production excellence with improved performance, productivity & compliance, as well as reduced losses & down-time, if they have KNOWLEDGE CONSISTENCY in all critical areas of manufacturing operations.

With 25 years in business, and offices in Europe, the USA and Canada, Skillpad has helped customers all over the world with Life Science Industry Knowledge challenges. We are fully dedicated to the idea that Knowledge Consistency is more achievable than ever using the latest technology and advanced knowledge transfer and management tools.

Ireland
USA
Canada
+353-1-687-0400
+1-973-588-4884
+1-514-316-2339

Get In Touch






    Records in API Manufacturing

    Effective record-keeping is a critical aspect of API manufacturing operations. This module introduces the essential records used in the manufacturing process, such as production, materials, laboratory, and distribution records. It emphasizes the importance of traceability, proper completion, and retention of records to ensure GMP compliance. Learners will explore common types of records, their content, and the rules for accurate documentation, enabling them to understand the role of records in maintaining product quality and ensuring regulatory compliance.

    Whether for onboarding or annual refresher training, this Module is seamlessly deployable on any LMS and can be tailored to your company’s exact needs.

      Duration: 30 Mins
    Grade: Core Library

    SKU: BGI-1101-SPL01-EN Categories: , Tag:

    Description

    • Understand the Purpose and Importance of Manufacturing Records: Gain comprehensive knowledge of the different types of records required in API manufacturing, including production, materials, laboratory, and maintenance records.
    • Build Enhanced Awareness of Traceability: Learn why maintaining accurate records is crucial for traceability in the production process, ensuring the ability to trace any issues back to their source.
    • Gain Critical Insights into Record Completion: Learn the rules for completing records, whether paper-based or electronic, including signature requirements, proper notation of errors, and retention timelines.
    • Knowledge of Regulatory Compliance: Develop a clear understanding of the importance of accurate documentation to meet GMP standards and the regulatory expectations for maintaining proper records throughout the manufacturing lifecycle.
    • Practical Guidance for Daily Operations: Equip yourself with the tools and techniques to complete records correctly and responsibly, ensuring compliance and product quality in every stage of production.

    Learning Objectives

    • Define ‘record’ as it relates to API manufacturing.
    • Explain why records are necessary in API manufacturing.
    • List examples of the types of records used in API manufacturing.
    • Explain why traceability is essential in API manufacturing.
    • Give examples of general rules for completing records.
    • List the information typically contained in production, materials, laboratory, and distribution records.
    • List the information typically contained in equipment maintenance and cleaning records

    Keywords

    • API Manufacturing
    • Batch Production Records
    • Cleaning Records
    • Documentation System
    • Equipment Maintenance
    • Equipment Sanitization
    • GMP Compliance
    • Laboratory Records
    • Materials Records
    • Product Traceability
    • Production Records
    • Quality Control
    • Record Completion
    • Record Retention
    • Record Rules
    • Regulatory Compliance
    • Sanitization
    • Traceability
    • Training Module
    • Validation Records

    Module Features

        Animations
       Voice Over
        Knowledge Checks
        Assessments
       SCORM/AICC compatible
        Full Screen

    Back To Top
    Your Cart

    Your cart is empty.