Regulatory Policies, Procedures and Prerequisites for Clinical Research
- Statistical issues in drug developmenrt
- Regulatory initiatives to promote the use of pharmacogenomics in drug development
- Investigation of new drugs
- Relevance of bioequivalence in approving generic copies of drug products
- Electronic regulatory submission and review
- Drug application regulatory compliance
- New drug quality assessment
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Regulatory Policies, Procedures and Prerequisites for Clinical Research Conference Speakers
Recommended Sessions
- Study Designs
- Advances in Assessment of Bioequivalence
- Bioanalytical Methodology
- Bioavailability, Bioequivalence and Drug Product Selection
- Clinical Pharmacology and Therapeutics
- Contemporary Challenges of Drug Design, Discovery and Development
- Emerging Bioavailability and Bioequivalence Studies
- Factors Affecting Bioavailability
- Managing BA/BE Studies
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- Need for Conducting BA/BE Studies
- Regulatory Policies, Procedures and Prerequisites for Clinical Research
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