Courses

FDA vs Health Canada - Similarities and Differences between the two Regulatory Bodies

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21 CFR PART 11 COMPLIANCE FOR ELECTRONIC RECORDS AND SIGNATURES

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Production and Process Controls for Medical Devices

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EU's New Regulation 535/2014 On Clinical Trials - Insights Into Effective Clinical Trials

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Good Clinical Practices Review of ICH E6 (R3) Latest Guidance

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Continued Process Verification and Process Monitoring

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FDA/ICH Guideline Q9 (R1) On Quality Risk Management

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3-Hour Virtual Seminar On IEC 62304 - Medical Device Software Compliance

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How to Deal with Bad Results Under GLP

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Medical Device Hazard Analysis following ISO 14971

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Top Process Validation Mistakes – And How to Avoid Them

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Quality in Technology Transfer Projects

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