Clinical Trial Regulations & GCP in Europe & UK

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Clinical Trial Regulations & GCP in Europe & UK

pharmaceutical business analytics distance course

Distance Learning

✔ ACCRE USA Accredited
✔ Program developed by senior industry experts
✔ eBooks – Presentation & Notes on Cliniminds LMS
✔ Cliniminds Certification after completion of program
✔ MCQ based final exams
✔ Introduction to Quality in Clinical Trials | Importance of quality | Quality control and assurance in research | Emphasis of QC and QA per ICH-GCP | Process mapping | Exercise | Audits | Definition | Types | Audit tools | Auditors | Audit preparation | Conduct of an Audit | Responding to Audit findings | Regulatory Inspections | FDA | EMEA | MHRA | ANVISA | DCGI | Fraud, Misconduct, and Errors | Definitions | Reasons | Types | Consequences with examples

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Clinical Trial Regulations & GCP in Europe & UK Course Details

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