Bioinformatics in Clinical Research
Bioinformatics in Clinical Research the typically controversial ethical issues emerging from new situations and possibilities brought about by advances in medicine. It is also moral discernment as it relates to medical policy, practice, and research. Bioethicists are concerned with the ethical questions that arise in the relationships among life sciences, biotechnology, medicine, clinical research, and philosophy etc. One of the first areas addressed by modern bioethicists was that of human experimentation. The National Commission for the Protection of Human Subjects of Biomedical and Behavioural Research was initially established in 1974 to identify the basic ethical principles that should underlie the conduct of biomedical and behavioral research involving human subjects.
Clinical research ethics are the set of relevant ethics considered in the conduct of a clinical trial in the field of clinical research. It borrows from the broader fields of research ethics and medical ethics. Quality of clinical trials depends on data integrity and subject protection. Good Clinical Practice (GCP) is the universal ethical and scientific quality standard for conducting clinical trials. The GCP standard applies to all aspects of the clinical trial process.
- Molecular epidemiology
- Pharmacogenetics and biomarkers
- Clinical molecular genetics
- Clinical forensic medicine.
- Patterns of drug utilization
- The effect of drug overdoses.
- The economic implications of drug use.
- Discovery undetected adverse and beneficial effects
- Reassurance about drug safety
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Bioinformatics in Clinical Research Conference Speakers
Recommended Sessions
- Clinical and Medical Case Reports
- Clinical Data Management
- Clinical Research & Clinical Trials: Academic Perspective
- Clinical Trials on Different Diseases
- CRO (Contract Research Organization) Clinical Trials
- Entrepreneurs Investment Meet
- Future Perspectives and Innovations in Clinical Studies
- Globalization of Clinical Trials
- Nano Technology in Clinical Trials
- Outsourcing and Collaborative Research in Clinical Trials
- Pharmacogenomics
- Pharmacovigilance and Drug Safety
- Bioinformatics in Clinical Research
- Clinical Trials Conducts
- Drug Discovery and Development
- Gastrointestinal oncology
- In Silico Clinical Trials
- Patient-Centric Clinical Trials
- Pharmacoepidemiology
- Research and Trials on Oncology and AIDS
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- Targeted Drug Delivery and Precision Medicine - Drug Delivery-2025 (France)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Spain)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Transdermal and Intradermal Delivery Systems - Drug Delivery-2025 (Netherlands)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Trending: Digital Health and Telemedicine for Rare Care - ORPHAN DRUGS 2025 (France)
- Types of Formulations - Formulations 2025 (France)
- Vaccine Delivery Technologies - Drug Delivery-2025 (Netherlands)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Veterinary Pharmacology - Pharmacology-2025 (Spain)
- Women in Rare Disease Leadership and Science - ORPHAN DRUGS 2025 (France)