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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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