Clinical Trial Protocols
An exploration convention is a record that depicts the foundation, reason, goals, outline, philosophy, factual contemplations, and association of a clinical research venture. As per the ICH Good Clinical Practice rules, a convention ought to incorporate the accompanying points:
Cover sheet (General Information)
Foundation Information
Destinations/Purpose
Study Design
Choice and Exclusion of Subjects
Treatment of Subjects
Appraisal of Efficacy
Appraisal of Safety
Unfriendly Events
Stopping of the Study
Measurements
Quality Control and Assurance
Morals
Information taking care of and Recordkeeping
Distribution Policy
Task Timetable/Flowchart
References
Supplements/Appendices
- Emerging technology in clinical trials
- Recent clinical trials on AIDS
- Research and Trials on Oncology and AIDS
- Clinical trials on benign and malignant tumors
- Clinical trials on cardiovascular diseases
- Clinical trials on diabetes
- Clinical trials of monoclonal and polyclonal antibodies
- Clinical trials on drugs used in psychological disorders
- Applications of biomarkers in clinical trials
- Clinical trials for Cancer
- Neurological Disorders
- Autoimmune Disorders
- Respiratory Disorders
- Chronic Diseases
Related Conference of Clinical Trial Protocols
Clinical Trial Protocols Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Biopharmaceutical Sciences
- Clinical Data Management and Analytics
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Trial Protocols
- Clinical Trial Site Selection and Management
- Diversity in Industrial Clinical Trials and Clinical Research
- Drug Safety
- Drugs Regulations
- Good Pharmacovigilance Practice
- Hospital and Indutrial Pharmacy
- Medical and Clinical Case Reports
- Pre-Clinical and Clinical Trials