Similarities between Food and Drug Administration and Postmarketing surveillance
Food and Drug Administration and Postmarketing surveillance have 7 things in common (in Unionpedia): Adverse drug reaction, Clinical trial, Health Canada, Medical device, Medication, Medicines and Healthcare products Regulatory Agency, MedWatch.
Adverse drug reaction
An adverse drug reaction (ADR) is an injury caused by taking a medication.
Adverse drug reaction and Food and Drug Administration · Adverse drug reaction and Postmarketing surveillance ·
Clinical trial
Clinical trials are experiments or observations done in clinical research.
Clinical trial and Food and Drug Administration · Clinical trial and Postmarketing surveillance ·
Health Canada
Health Canada (Santé Canada) is the department of the government of Canada with responsibility for national public health.
Food and Drug Administration and Health Canada · Health Canada and Postmarketing surveillance ·
Medical device
A medical device is any apparatus, appliance, software, material, or other article—whether used alone or in combination, including the software intended by its manufacturer to be used specifically for diagnostic and/or therapeutic purposes and necessary for its proper application—intended by the manufacturer to be used for human beings for the purpose of.
Food and Drug Administration and Medical device · Medical device and Postmarketing surveillance ·
Medication
A medication (also referred to as medicine, pharmaceutical drug, or simply drug) is a drug used to diagnose, cure, treat, or prevent disease.
Food and Drug Administration and Medication · Medication and Postmarketing surveillance ·
Medicines and Healthcare products Regulatory Agency
The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
Food and Drug Administration and Medicines and Healthcare products Regulatory Agency · Medicines and Healthcare products Regulatory Agency and Postmarketing surveillance ·
MedWatch
MedWatch is the Food and Drug Administration’s Safety Information and Adverse Event Reporting Program.
Food and Drug Administration and MedWatch · MedWatch and Postmarketing surveillance ·
The list above answers the following questions
- What Food and Drug Administration and Postmarketing surveillance have in common
- What are the similarities between Food and Drug Administration and Postmarketing surveillance
Food and Drug Administration and Postmarketing surveillance Comparison
Food and Drug Administration has 214 relations, while Postmarketing surveillance has 18. As they have in common 7, the Jaccard index is 3.02% = 7 / (214 + 18).
References
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