Health technology assessment
Health technology assessment (HTA) is that the systematic evaluation of the properties and effects of a health technology, addressing the direct and intended effects of this technology, also as its indirect and unintended consequences, and aimed mainly at informing deciding regarding health technologies. it's other definitions including a way of evidence synthesis that considers evidence regarding clinical effectiveness, safety, cost-effectiveness and, when broadly applied, includes social, ethical, and legal aspects of the utilization of health technologies. The precise balance of those inputs depends on the aim of every individual HTA. a serious use of HTAs is in informing reimbursement and coverage decisions by insurers and national health systems, during which case HTAs should include benefit-harm assessment and economic evaluation. and a multidisciplinary process that summarises information about the medical, social, economic and ethical issues associated with the utilization of a health technology during a systematic, transparent, unbiased, robust manner. Its aim is to tell the formulation of safe, effective, health policies that are patient focused and seek to realize best value. Despite its policy goals, HTA should be firmly rooted in research and therefore the methodology.
- Health technology assessment (HTA)
- Effects of this technology
- cost-effectiveness
- utilization of health technologies
- economic evaluation
- information about the medical, social, economic and ethical issues
Related Conference of Health technology assessment
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Health technology assessment Conference Speakers
Recommended Sessions
- Causality Assessment
- Global Clinical Trials
- Adverse Drug Reactions
- Analysis of Data Quality and Management
- Biopharmaceutics
- Clinical Database Management
- Clinical Research and Statistics
- Clinical Trial Protocols
- Clinical Trials Pharmacovigilance
- Drug related problems in healthcare
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- Orphan drugs
- Pharmaceutical Chemistry
- Pharmaceutical Formulation
- Pharmaceutical Nanotechnology
- Pharmacokinetics and Pharmacodynamics in Drugs
- Pharmacovigilance and Clinical Trials
- Pharmacovigilance Practice
- Pharmacovigilance Significance and Scope
- Regulatory Affairs
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- Regulatory updates on Biosimilars - Eurobiosimilars 2026 (Italy)
- Rehabilitation and Physical Therapy in Pain - Pain Management 2026 (France)
- Risk-Based Monitoring and Trial Optimization - Clinical Trials-2026 (UK)
- Safety Pharmacology - Pharmacology 2026 (Italy)
- Safety Reporting in Early Phase Trials - Clinical Trials-2026 (UK)
- Semi-Solid Dosage Forms - Formulations 2025 (France)
- Sexually Transmitted Bacterial Infections and Resistance Trends - Euro Antibiotics 2025 (Netherlands)
- Signal Prioritization and Management Techniques - Clinical Trials-2026 (UK)
- Single-Use Technologies in Production - Biologics Meet 2026 (UK)
- Site Management Innovation - Clinical Research 2026 (UK)
- Smart Drug Delivery Systems - Formulations 2025 (France)
- Solid Dosage Forms - Formulations 2025 (France)
- Stem Cell and Genetic Clinical Research - Clinical Research 2026 (UK)
- Stewardship Programs in Human and Animal Health - Euro Antibiotics 2025 (Netherlands)
- Structure-Based Drug Design and Molecular Docking - Euro MedChem and CADD 2025 (France)
- Supply Chain Management - Pharmaceuticals-2025 (France)
- Sustainable Antibiotic Practices and Global Policy - Euro Antibiotics 2025 (Netherlands)
- Sustainable Biologics Manufacturing - Biologics Meet 2026 (UK)
- Synthetic and Bioorganic Chemistry - PHARMACEUTICAL CHEMISTRY 2025 (France)
- Synthetic and Green Medicinal Chemistry - Euro MedChem and CADD 2025 (France)
- Systems Pharmacology and Drug Modeling - Euro Pharmacology 2025 (France)
- Target Identification and Validation - Euro MedChem and CADD 2025 (France)
- Targeted Drug Delivery and Nanomedicine in Infectious Diseases - Euro Antibiotics 2025 (Netherlands)
- Targeted Therapies - Personalizedmedicine-2025 (Switzerland)
- Technology in Pharma Sciences - MedTech-2025 (Switzerland)
- Telemedicine - Personalizedmedicine-2025 (Switzerland)
- The Role of CROs in Clinical Trial Execution - Clinical Trials-2026 (UK)
- Toxicological Impacts of Air and Water Pollution - Euro Pharmacology 2025 (France)
- Toxicology - Pharmacology 2026 (Italy)
- Toxicology and Safety Pharmacology - Pharmacology-2025 (Germany)
- Toxicology: Mechanisms and Risk Assessment - Euro Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2026 (Italy)
- Vaccine Development Against Bacterial Pathogens - Euro Antibiotics 2025 (Netherlands)
- Vaccines & Immunotherapy - Pharma Expo-2026 (Thailand)
- Veterinary Pharmacology - Pharmacology-2025 (Germany)