Drug Safety
Drug Safety heavily focuses on adverse drug reactions which are defined as any response to a drug which is noxious and unintended, including lack of efficacy. Medication errors such as overdose, and misuse and abuse of a drug as well as drug exposure during pregnancy and breastfeeding, are also of interest, even without an adverse event, because they may result in an adverse drug reaction. Information received from patients and healthcare providers via pharmacovigilance agreements (PVAs), as well as other sources such as the medical literature, plays a critical role in providing the data necessary for pharmacovigilance to take place. Ultimately, drug safety is concerned with identifying the hazards associated with pharmaceutical products and with minimizing the risk of any harm that may come to patients. Companies must conduct a comprehensive drug safety and pharmacovigilance audit to assess their compliance with worldwide laws, regulations, and guidance.
Related Conference of Drug Safety
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Drug Safety Conference Speakers
Recommended Sessions
- Adverse Drug Reactions
- Drug Delivery and Design Development
- Drug Delivery Technologies Pharmaceutical Delivery
- Drug Design with the Help of Computers (CADD)
- Drug discovery and Development
- Drug Discovery and Nanotechnology
- Drug Safety
- Forensic Science and Toxicology
- Pharmaceutical Drug Discovery and Nanotechnology
- Pharmacovigilance and Risk Management
- Pharmacy Computer Applications
- Regulatory Affairs
- Research and development in the pharmaceutical industry
- Science of Pharmaceuticals
- The Role of Medicinal Chemistry in Drug Development
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