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The People's Dispensary for Sick Animals (PDSA) is the UK's leading veterinary charity, carrying out more than one million free veterinary consultations a year.It was founded in 1917 by Maria Dickin to provide care for sick and injured animals of the poor.
The VENOM codes comprise an extensive, standardised list of terms for recording the best available diagnosis at the end of an animal visit. It comprises mainly diagnoses but also includes terms appropriate for administrative transactions (e.g. non prescription diet sales, over the counter items, travel related items) and preventive health visits (vaccination(s), routine parasite control ...
PDSA may refer to: PDSA (plan–do–study–act), a quality improvement process; People's Dispensary for Sick Animals, a UK veterinary charity;
After a request comes in from a qualified provider, the request will go through the prior authorization process. The process to obtain prior authorization varies from insurer to insurer but typically involves the completion and faxing of a prior authorization form; according to a 2018 report, 88% are either partially or entirely manual.
Maria Elisabeth Dickin CBE (nickname Mia; 22 September 1870 – 1 March 1951) was a social reformer [1] and an animal welfare pioneer who founded the People's Dispensary for Sick Animals (PDSA) in 1917. The Dickin Medal is named for her.
Predating modern legal definitions of a prescription, a prescription traditionally is composed of four parts: a superscription, inscription, subscription, and signature. [48] The superscription section contains the date of the prescription and patient information (name, address, age, etc.). The symbol "℞" separates the superscription from the ...
The Physicians' Desk Reference (PDR), renamed Prescriber's Digital Reference after its physical publication was discontinued, is a compilation of manufacturers' prescribing information (package insert) on prescription drugs, updated regularly and published by ConnectiveRx. [citation needed]
Prior to the Prescription Drug User Fee Act (PDUFA), median approval times of New Drug Applications ranged between 21 and 29 months. [2] The Prescription Drug User Fee Act was first passed in 1992 to facilitate the funding of the Food and Drug Administration while ensuring a more predictable timetable for drug approvals. [3]