Fundamentals of Clinical Research

Understand the basics of clinical trials.

Clinical Trial Management

Learn to manage clinical trials effectively.

Ethics in Clinical Research

Study ethical considerations in research.

Statistical Methods in Research

Learn statistical techniques for data analysis.

Review Protocol

Evaluating study protocols to ensure compliance and feasibility

Introduction to Clinical Data Management

Understand the fundamentals of data management.

Data Collection Techniques

Explore techniques for effective data collection.

Data Analysis in Clinical Research

Learn data analysis skills for clinical studies.

Database Design for Clinical Trials

Understand how to design databases for trials.

Data Validation

Ensuring accuracy, consistency, and integrity of clinical and operational data.

Discrepancy Management

Identifying, tracking, and resolving data inconsistencies efficiently.

Vendor & SAE Reconciliation

Aligning vendor data with safety reports for compliance and accuracy.

CDASH & SDTM

Standardizing clinical data for regulatory submissions and seamless analysis.

Introduction to Pharmacovigilance

Learn the basics of pharmacovigilance.

Adverse Event Reporting

Master the process of reporting adverse events.

Risk Management in Pharmacovigilance

Explore risk management strategies for drug safety.

Pharmacovigilance Regulations

Understand the regulatory environment for pharmacovigilance.

Introduction to Regulatory Affairs

Learn the fundamentals of regulatory affairs.

Compliance in Clinical Trials

Master compliance requirements in clinical research.

Regulatory Submissions and Approvals

Understand the submission process for approvals.

Regulatory Compliance Audits

Explore the auditing process for compliance.