What does PAM mean in VETERINARY
Postapproval Monitoring (PAM) is the process of monitoring the safety and effectiveness of a product after it has been approved for marketing and sale. PAM is used to ensure products meet their expected performance criteria, as stated in the applicable regulations or guidance documents.
PAM meaning in Veterinary in Medical
PAM mostly used in an acronym Veterinary in Category Medical that means Postapproval Monitoring
Shorthand: PAM,
Full Form: Postapproval Monitoring
For more information of "Postapproval Monitoring", see the section below.
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Essential Questions and Answers on Postapproval Monitoring in "MEDICAL»VET"
What is Postapproval Monitoring (PAM)?
Why is PAM important?
PAM is important because it helps to protect consumers from potential risks associated with the use of a particular product or device. By monitoring products post-approval, regulators can identify any unexpected issues that may arise once they enter the market. PAM also helps to reduce risk by ensuring that approved products comply with their intended purpose and performance claims.
What types of PAM are there?
There are several different types of postapproval monitoring as it may differ depending on the type of product being monitored. Common types of PAM include adverse event reporting, recalls, engineering checks, clinical trials, field studies, laboratory testing, surveys and market research.
What does adverse events reporting involve?
Adverse event reporting involves tracking reports of unexpected serious harm caused by an approved product or device after its release for sale to consumers. Adverse events can range from minor symptoms such as nausea or headaches to more serious events like death or disability. Reports are then reviewed and investigated by regulatory authorities for further follow up action if necessary.
What kind of data is collected during PAM?
Different types of data are collected during postapproval monitoring depending on the type and complexity of the product being monitored. This could include but not limited to customer feedback surveys, laboratory tests results, investigation reports on adverse events, etc. All data collected will be analyzed according to established practices and procedures in order to detect any potential safety risks associated with the use of a particular product or device.
Who conducts Postapproval Monitoring activities?
Generally speaking, various entities have involvement in conducting postapproval monitoring activities for a particular product or device. This may include manufacturers themselves who have an obligation under applicable laws to monitor their products closely after they enter into market; regulatory authorities who are responsible for assessing these manufacturers’ compliance with regulations; as well as other health care providers who have direct contact with patients using those products/devices.
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