Clinical Database Management
Track 10: Clinical Database Management
The field of clinical knowledge management (CDM) has manifested itself thanks to demands from each the pharmaceutical business and therefore the restrictive authorities. Because the drive to “fast-track” the event of pharmaceutical product continues to accelerate, restrictive entities have responded by requiring quality-assurance standards be met in assembling the info employed in the drug analysis method. Clinical knowledge management systems (CDMS) area unit particularly important in trials conducted across medical centres during which a colossal quantity of information is made.
- Non-Drug Therapy
- Pharmaceutical Things
- Role of clinical data management in clinical trial
- Data Management plan in CDM
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Clinical Database Management Conference Speakers
Recommended Sessions
- Pharmaceutical Research and Development
- Adverse Drug Reactions
- Causality Assessment
- Clinical Data Management
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Research Nursing
- Clinical Trial Protocols
- Clinical Trials Pharmacovigilance
- Drug Delivery Technologies & Drug Designing and Development
- Drug repurposing to treat Viruses: COVID-19
- Drug Safety
- Drug Safety and Pharmacovigilance
- Global Clinical Trials
- Importance of Audit in Pharmaceutical Industry
- Medical Devices for Drug Delivery
- Pharma Market Research
- Pharmaceutical Nanotechnology: Challenges and Opportunities
- Pharmacoeconomics
- Pharmacokinetics and Pharmacodynamics in Drugs
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance and Cosmetovigilance
- Pharmacovigilance and Risk Management
- Pharmacovigilance Practice
- Pharmacovigilance Significance and Scope
- Prevalence of Potential Drug- Drug Interaction
- Recent trends in Pharma and Technology
- Regulatory Authority Compliance
- Track: 29 Oncology Clinical Research
- Track:30 Risk assessment and management in clinical trials
- Use of Nanoparticles in DDS and Newer Methodologies
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- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Track 01: Digital Marketing in Pharma Industry - Future Pharma 2026 (Netherlands)
- Track 02: The Future of Pharma R&D - Future Pharma 2026 (Netherlands)
- Track 03: Pharmaceutical Chemistry - Future Pharma 2026 (Netherlands)
- Track 04: Pharmaceutical Analysis - Future Pharma 2026 (Netherlands)
- Track 05: Pharmaceutics & Pharmacotherapeutics - Future Pharma 2026 (Netherlands)
- Track 06: Industrial Pharmacy and Physical pharmacy - Future Pharma 2026 (Netherlands)
- Track 07: Clinical and Hospital Pharmacy - Future Pharma 2026 (Netherlands)
- Track 08: Pharmaceutical and healthcare Industry - Future Pharma 2026 (Netherlands)
- Track 09: Regulatory Affairs and Intellectual Property Rights - Future Pharma 2026 (Netherlands)
- Track 10: Pharma and Biotech Financial Outlook - Future Pharma 2026 (Netherlands)
- Track 11: Novel Drug Delivery Systems - Future Pharma 2026 (Netherlands)
- Track 12: Drug Discovery and Development - Future Pharma 2026 (Netherlands)
- Track 13: Green and Community Pharmacy - Future Pharma 2026 (Netherlands)
- Track 14: Big data analytics and Pharma - Future Pharma 2026 (Netherlands)
- Transdermal and Intradermal Delivery Systems - Drug-Delivery-2026 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Delivery Technologies - Drug-Delivery-2026 (France)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)