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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.


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    Records in Finished Dose Manufacturing

    This Module is aimed at personnel who work in the pharmaceutical and biopharmaceutical industries and maintain records for finished dose manufacturing in accordance with GMP Regulations, including records of materials, production records, equipment records, laboratory records, production review and distribution records.

      Duration: 30 Mins

    SKU: PGI-1101-SPL03-EN Categories: , , Tag:


    Learning Objectives:

    • Explain why records are essential in finished dose manufacturing
    • List examples of the types of records used in finished dose manufacturing
    • Explain why traceability is essential in finished dose manufacturing
    • Define ‘record’ as it relates to finished dose manufacturing
    • Give examples of general rules for completing record
    • List the information typically contained in production, materials, laboratory, and distribution records
    • List the information typically contained in equipment use, maintenance, and cleaning/sterilization records
    Module Features:

       Voice Over
        Knowledge Checks
       SCORM/AICC compatible
        Full Screen

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