📊 What is Clinical Data Management (CDM)?
Clinical Data Management (CDM) ensures that data collected during clinical research is accurate, reliable, and secure for analysis. It includes:
- Collecting, entering, cleaning, and processing data
- Adhering to regulatory guidelines
- Maintaining data integrity for regulatory submissions and medical decisions
CDM is essential in clinical trials, helping researchers manage data throughout the study. With advanced software tools, CDM minimizes errors and missing data, efficiently tracks changes, and resolves discrepancies. As trials grow in scale and complexity, CDM becomes increasingly vital.
🚀 Why You Should Enroll in This Course
- The Indian pharmaceutical industry is booming, integrating AI, machine learning, and cloud-based systems.
- India’s strong IT infrastructure and cost-effective solutions make it a global hub for clinical research outsourcing.
- The global CDM market is projected to reach USD 5.76 billion by 2030, growing at a CAGR of 11.5%.
- Rising demand for skilled professionals opens doors in:
- Pharmaceutical companies
- Contract Research Organizations (CROs)
- Biotechnology firms
- Healthcare IT sectors
- High-demand roles include:
- Clinical Data Manager
- Data Analyst
- Regulatory Specialist
🎓 Who Should Apply?
Applicants must have at least 50% in graduation and hold a degree in one of the following fields:
| Category | Eligible Degrees |
| Doctors | BDS, BAMS, BHMS, BUMS, Pharmacology |
| Life Sciences/Biosciences | B.Sc., M.Sc., Biomedical, Biotech, Microbiology, Medical Lab Science |
| Pharmacy | B.Pharm, M.Pharm, PharmD |
| Nursing/Allied Health | BPT, OT, Nursing |
📘 Focus of the Program
- Clinical data management workflow
- Code of Federal Regulations (CFR) and regulatory guidelines
- Case Report Forms (CRFs) – paper and electronic (eCRFs)
- Protocol design for clinical trials
- Data integrity, validation, and standardization
- Good Clinical Practice (GCP) and ICH guidelines
- Statistical Analysis System (SAS) and Electronic Data Capture (EDC) systems
🛠️ Skills You Will Learn
- CDM setup, conduct, and closeout procedures
- Database locking and regulatory compliance
- Medidata Rave and other CDM software tools
- Best practices in clinical trial data management
- Query management and discrepancy resolution
- CDISC standards (SDTM & ADaM) for data submission
- Clinical data analysis and reporting
📝 How to Apply
You can apply for the Clinical Data Management Certification Course directly through our website. Once your application is received, our team will guide you through the next steps.
📞 Call Us: +91 [Insert Number]
💬 WhatsApp: +91 [Insert Number]
Mail – clinicaledutech@gmail.com