Distance Learning

Advanced Post Gradaute Diploma in Clinical Research, Pharmacovigilance & Clinical Data Management

✔ 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
✔ Drug Discovery | Overview of Clinical Research | Regulations & Guidelines | Roles & Responsibilities | Preparation & Planning of Clinical Trials | Essential Documentation & Regulatory Submission | Study Start-Up Process | Clinical Monitoring Essentials | Compliance, Auditing & Quality Control | Overview of Clinical Research | Pharmacology – General Principles | Introduction to Pharmacovigilance | Pharmacovigilance Regulations | Hands-On Training on Case Processing and Report Generation | Safety Reporting and Processing ICSR | Aggregate Reports, Signal Detection & Risk Management | Documents in Pharmacovigilance | Audits & Inspections | Advanced Pharmacovigilance & Analytics | Overview of Clinical Data Management | Clinical Data Integrity | Data Management Plan | Design of Case Report Form | CRF Tracking | Electronic Data Capture | Data Entry Guidelines | Edit Check Creation, Validation, Programming | Discrepancy Management | Data Transfer | Medical Coding Dictionaries | Laboratory Test in Clinical Trials | Creating Reports | Adverse Event Reporting & Reconciliation | Audit Trail | Database Lock | Quality Assurance | QMS, Audit & Inspection, SOP Compliance | Hands-On Software Training