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Mastering Batch Record Review – Level 1
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May 15, 2025
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Future-Proofing Clinical Trials: Essential GCP Updates You Need to Know (FREE)
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May 16, 2025
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Mastering GCP Innovations: Implementing ICH E6(R3) in Modern Clinical Trials
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May 29, 2025
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Drug Product Submission (NDS) Preparation in CTD and eCTD Format Workshop – Level 3
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May 30, 2025
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Mergers & Acquisitions (Due Diligence to Execution) – A Regulatory Perspective
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June 5, 2025
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Computer System Validation (CSV) Essentials: Ensuring Compliance in Regulated Sectors (FREE)
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June 12, 2025
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Navigating the USP: Practical Guidance for QA, QC and Industry Professionals
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June 18, 2025
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Mastering Batch Record Review: Ensuring GMP Compliance and Quality – Level 2
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June 19, 2025
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Computer System Validation (CSV) – Introduction to General Principles
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June 26, 2025
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