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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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    Overview of Biopharmaceutical Manufacturing

    This Module is aimed at biopharmaceutical manufacturing personnel who require an overview of the main processes and conditions involved in therapeutic protein manufacture including upstream processing, downstream processing as well as formulation and fill finish.

    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

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    SKU: BPU-1105-SPL06-EN Category: Tag:

    Description

    Learning Objectives:

    • Describe the main types of biopharmaceutical products
    • Explain why following GMP is critical in biopharmaceutical manufacturing
    • Explain why aseptic processing and clean rooms are critical in biopharmaceutical manufacturing
    • Explain the terms CIP and SIP and their importance in a biopharmaceutical manufacturing process
    • Describe the different stages of upstream processing
    • Describe the different stages of downstream processing
    • Explain the purpose of product formulation

    Learner Benefits:

    • Gain a thorough understanding of the biopharmaceutical manufacturing process, from the initial cell cultivation to the final product formulation and packaging.
    • Enhance your knowledge of relevant Good Manufacturing Practices (GMP), ensuring adherence to industry standards and regulatory requirements for biopharmaceutical production.
    • Understand the importance of aseptic processing, cleanrooms, and the critical measures needed to control microbial contamination throughout the manufacturing process.
    • Develop a strong grasp of upstream and downstream processing stages, including key contamination control measures such as CIP (Clean-In-Place) and SIP (Steam-In-Place).
    		 Module Features:

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

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