Pre-Clinical and Clinical Trials
Pre-Clinical and Clinical Trials aim at testing the potentiality of medicinal therapeutic efficacy of pharmaceutical products on cells and animals. Clinical study design aims to ensure the scientific validity and reproducibility of the results. Clinical trials is the propagative studies conducted on patients using of patient data, disease mechanisms, therapeutic interventions and epidemiology, patient centric approach and benefit risk management. Pre-Clinical trials are essential before a company starts performing the clinical trials and helps in calculating toxicity, efficacy and collecting pharmacokinetic data. Pre-Clinical and Clinical Trials involve intervention of human subjects to study the cause-and-effect relationship between a medical intervention and a health outcome. The perfect outcome of clinical trials is minimizing risks; enhance benefits, and optimal use of an intervention of therapeutic drugs.
- Bioassay and its types
- Pre-Clinical Testing
- Phases of Clinical Research
- Drug Development
- Placebo groups
- Regulatory agencies
- Clinical trial protocol
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- Toxicology - Pharmacology 2025 (France)
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