Clinical Trials 2024 | Vancouver | Canada| Clinical Trials Conferences

Bioethics, Quality Regulation and Case Reports

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Bioethics is the study of 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 Behavioral 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.

Improvements in FDA review process efficiency and more frequent and timely interactions with FDA Overall; the therapeutic area with the highest clinical research burden across all phases is respiratory system ($115.3 million) followed by pain and anaesthesia ($105.4 million) and oncology ($78.6 million) trials. Use of lower-cost facilities/in-home testing and wider use of mobile technologies appear to be most effective in reducing costs across therapeutic areas and trial phases. Use of lower-cost facilities and/or in-home testing can reduce per-trial costs by up to $0.8 million (16 percent) in Phase 1, $4.3 million (22 percent) in Phase 2, and $9.1 million (17 percent) in Phase 3, depending on therapeutic area

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. Globalization, outsourcing and increasing complexity of clinical trials have made the target of achieving global quality challenging. The quality, as judged by regulatory inspections of the investigator sites, sponsors/contract research organizations and Institutional Review Board, has been of concern to the US Food and Drug Administration, as there has been hardly any change in frequency and nature of common deficiencies. 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.

Compliance and regulatory requirements in clinical research
Ethical regulatory guidelines
Capacity building in clinical research
Bioethics: Case studies
Pharmacokinetics-Pharmacodynamics for regulatory decision
Ethical and regulatory issues

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November 25-26, 2024

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Radiation-based medicines and biotherapy - Drug Safety 2024 (France)
Rational Design of Non-Oral Drugs - PHARMA MEDICINAL CHEMISTRY 2025 (Canada)
Rational Drug Design and Molecular Modeling - PHARMA CONFERENCE-2025 (Czech Republic)
Real-World Evidence in Clinical Trials - Pharma Europe 2025 (Italy)
Recent Advancements in Medicinal Pharma - PHARMA MEDICINAL CHEMISTRY 2025 (Canada)
Reformulation Research - Drug Safety 2024 (France)
Regenerative Medicine and Tissue Engineering - Drug Delivery-2024 (France)
Regulatory Affairs and Drug Safety - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
Regulatory Affairs and Intellectual Property Rights - Future Pharma 2025 (Netherlands)
Regulatory Affairs and Quality Assurance in Pharmaceutics - Pharmaceutica-2025 (Canada)
Regulatory Authority Compliance - MedTech-2024 (Switzerland)
Regulatory Considerations in Drug Development - Drug Delivery-2024 (France)
Regulatory Requirements for Pharmaceuticals - PHARMACEUTICAL SCIENCES 2025 (France)
Regulatory Updates on Biosimilars - Eurobiosimilars 2025 (France)
Research and development in pharmaceuticals - Drug Safety 2024 (France)
Research and Trials on Oncology and AIDS - Clinical-Trials-2024 (Canada)
Role of Gut Microbiome in Cardiovascular Health - Cardiovascular-2025 (France)
Role of Inflammation in Cardiovascular Diseases - Cardiovascular-2025 (France)
Safety of drugs and pharmacovigilance - Drug Safety 2024 (France)
Smart Drug Delivery Systems - Pharmatech 2025 (Canada)
Smart Polymers for Drug Delivery - Pharmaceutica-2025 (Canada)
Sustainability and Global Health Biotechnology - Biotech-2025 (France)
Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (Italy)
Targeted Drug Delivery and Controlled Release Systems - PHARMA CONFERENCE-2025 (Czech Republic)
Targeted Therapies - Personalizedmedicine-2024 (Switzerland)
Targeted Therapies in Cardiovascular Regeneration - Cardiovascular-2025 (France)
Targeting the Renin-Angiotensin-Aldosterone System (RAAS) - Cardiovascular-2025 (France)
Technologies for Formulation - Drug Safety 2024 (France)
Technology in Pharma Sciences - MedTech-2024 (Switzerland)
Telemedicine - Personalizedmedicine-2024 (Switzerland)
The BBB for drug delivery - Drug Safety 2024 (France)
The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
The Next Generation Approach of Antibiotics - Antibiotics Resistance 2024 (Canada)
Therapeutic Drug Transporters - Drug Safety 2024 (France)
Translational Research - Personalizedmedicine-2024 (Switzerland)
Translational Research in Pharmacology and Therapeutics - NURSING PHARMACOLOGY 2024 (Netherlands)
USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (Czech Republic)
Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (Czech Republic)

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