Clinical Trials
The main goals of Pre-Clinical and Clinical Trials are to determine the safe dose and start to assess product's safety profile. Concentrating on dosages forms in random clinical trials is very important. Although preclinical studies have revealed many possible mechanisms for these Adverse Events, the causes of some adverse events remain unknown.
Discussions are encouraged on Preclinical and clinical trial mechanisms and their significance, improvements, adversity.
- Discovery and Preclinical Testing Phases
- Pre-Clinical Testing
- Clinical Study Designs
- Bioassay and its types
- Data collection and quality control
- Alternative trials design and models
- Multi center trials and monitoring
- Regulatory authorities and ethics committee
- Advanced Information technology in clinical trials and promoting companies
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Clinical Trials Conference Speakers
Recommended Sessions
- Adverse Drug Reaction
- Challenges in Pharmacy Practice
- Clinical and Medical Case Reports
- Clinical Data Management and Statistics
- Clinical Research
- Clinical Trails on Various Disorders
- Clinical Trials
- Drug Safety
- Good Pharmacovigilance Practice
- Innovations in Clinical Trials
- Innovations in Pre-clinical Research
- Pharmaceutical Toxicology
- Pharmacokinetics and Pharmacodynamics
- Pharmacovigilance and Risk Management
- Pharmacovigilance Significance & Scope
- Regulatory Affairs
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