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Dosage forms (also called unit doses) are pharmaceutical drug products presented in a specific form for use. They contain a mixture of active ingredients and inactive components (), configured in a particular way (such as a capsule shell) and apportioned into a specific dose.
In the countries of the UK, National Health Service (NHS) prescriptions are either free or have a fixed price per item; [43] a prescription may be issued so the patient does not have to purchase the item at commercial price. Some medical software requires a prescription. [44] Legislation may define certain equipment as "prescription devices". [45]
Pharmaceutical Representative is a trade journal featuring common sales tactics such as how to close a tough sale by flattering a stubborn doctor. [9] Along with flattery, the attractiveness of sales reps has been noted, with a trend of former cheerleaders entering the field.
Authorized generics are prescription drugs produced by brand pharmaceutical companies and marketed under a private label, at generic prices. Authorized generics compete with generic products in that they are identical to their brand counterpart in both active and inactive ingredients; [1] whereas according to the U.S. Food and Drug Administration's Office of Generic Drugs, generic drugs are ...
"Drugs and Cosmetics Rules, 1945" (PDF). Central Drugs Standard Control Organization.Archived from the original (PDF) on 31 October 2005.; A Review on the Current Classification and Regulatory Provisions for Medicines in Drug & Cosmetic Act, in the light of Present Day Context Recommendations for Drugs & Cosmetics Rules with context of Drug Schedules
An Abbreviated New Drug Application (ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug.. The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product.
When an authenticated consumer tries to access a resource, the access control process checks that the consumer has been authorized to use that resource. Authorization is the responsibility of an authority , such as a department manager, within the application domain, but is often delegated to a custodian such as a system administrator.
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