Pharmacokinetics
Pharmacokinetics is the study of the dynamic motions of foreign substances, sometimes known as xenobiotics, as they transit through the body. It involves the kinetics of absorption, distribution, biotransformation/metabolism, and excretion (ADME). It's basically how the body reacts to xenobiotics. We can better comprehend, analyse, and even foresee the kind and extent of the biological effects of xenobiotics thanks to the field of pharmacokinetics, which uses mathematical equations to represent the time course of ADME of xenobiotics in the body. Pharmacokinetics is one way used to describe the fate of xenobiotics in the body, and it views the body as one or more homogeneous compartments based on either mathematical fitting or physiological properties.
Related Conference of Pharmacokinetics
7th World Congress on Advanced Clinical Trials and Clinical Research
4th International Forum on Pharmacovigilance and Regulatory Affairs
Pharmacokinetics Conference Speakers
Recommended Sessions
- Pharmacology
- Adverse drug reactions
- Autonomic Pharmacology
- Cardiovascular Pharmacology
- Clinical Pharmacology
- Drug Discovery and Drug Screening
- Environmental Pharmacology
- Ethnopharmacology
- Forensic Toxicology
- Genetic Toxicology
- Neuropharmacology
- Nursing Pharmacology
- Pharmaceutical Chemistry
- Pharmacodynamics
- Pharmacokinetics
- Pharmacological Testing
- Psychopharmacology
- Toxicology
Related Journals
Are you interested in
- Adaptive Trial Models - Clinical Trials Congress 2025 (Spain)
- Advanced Data Analytics - Clinical Trials Congress 2025 (Spain)
- Adverse Event Reporting through Mobile Health Tools - Euro Pharmacovigilance 2025 (Spain)
- AI in Clinical Research - Clinical Trials Congress 2025 (Spain)
- AI-Driven Signal Detection and Data Mining - Euro Pharmacovigilance 2025 (Spain)
- AI-Powered Pharmacovigilance - Clinical Trials Congress 2025 (Spain)
- Automation in Case Processing and Reporting - Euro Pharmacovigilance 2025 (Spain)
- Blockchain Applications - Clinical Trials Congress 2025 (Spain)
- Blockchain Applications in Regulatory Data Integrity - Euro Pharmacovigilance 2025 (Spain)
- Clinical Supply Chain Innovation - Clinical Trials Congress 2025 (Spain)
- Data Integrity & Compliance - Clinical Trials Congress 2025 (Spain)
- Decentralized Trials - Clinical Trials Congress 2025 (Spain)
- Digital Therapeutics Trials - Clinical Trials Congress 2025 (Spain)
- Digital Transformation in Drug Safety Operations - Euro Pharmacovigilance 2025 (Spain)
- Diversity in Enrollment - Clinical Trials Congress 2025 (Spain)
- eConsent & Retention Tools - Clinical Trials Congress 2025 (Spain)
- eSource & EDC Systems - Clinical Trials Congress 2025 (Spain)
- Ethics and Legal Challenges in Drug Safety Surveillance - Euro Pharmacovigilance 2025 (Spain)
- Global Harmonization of Regulatory Frameworks - Euro Pharmacovigilance 2025 (Spain)
- Global Regulatory Landscape - Clinical Trials Congress 2025 (Spain)
- Global Signal Management Systems and Standards - Euro Pharmacovigilance 2025 (Spain)
- Inspection Readiness and Audit Best Practices - Euro Pharmacovigilance 2025 (Spain)
- Integration of PV with Quality and Regulatory Affairs - Euro Pharmacovigilance 2025 (Spain)
- Managing Safety Data in Multi-Region Submissions - Euro Pharmacovigilance 2025 (Spain)
- Master Protocol Strategies - Clinical Trials Congress 2025 (Spain)
- Patient-Centric Designs - Clinical Trials Congress 2025 (Spain)
- Patient-Centric Pharmacovigilance Strategies - Euro Pharmacovigilance 2025 (Spain)
- Pharmacovigilance Compliance in Clinical Trials - Euro Pharmacovigilance 2025 (Spain)
- Pharmacovigilance in Accelerated Drug Approvals - Euro Pharmacovigilance 2025 (Spain)
- Pharmacovigilance in Gene and Cell Therapies - Euro Pharmacovigilance 2025 (Spain)
- Pharmacovigilance Outsourcing and Vendor Oversight - Euro Pharmacovigilance 2025 (Spain)
- Real-World Evidence in Post-Marketing Surveillance - Euro Pharmacovigilance 2025 (Spain)
- Real-World Evidence Integration - Clinical Trials Congress 2025 (Spain)
- Risk Management Planning and Benefit-Risk Assessment - Euro Pharmacovigilance 2025 (Spain)
- Risk-Based Monitoring - Clinical Trials Congress 2025 (Spain)
- Safety Labeling Changes and Regulatory Communication - Euro Pharmacovigilance 2025 (Spain)
- Safety Monitoring of Biologics and Biosimilars - Euro Pharmacovigilance 2025 (Spain)
- Synthetic Control Arms - Clinical Trials Congress 2025 (Spain)
- Virtual Trial Platforms - Clinical Trials Congress 2025 (Spain)
- Wearables & Remote Monitoring - Clinical Trials Congress 2025 (Spain)