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(February 22, 2019, Rev.)COMMONWEALTH OF PENNSYLVANIA DEPARTMENT OF HEALTH(Formerly form H114.120/H114.614)Application for Registration under the Drug, Device and Cosmetic Act and Licensure under
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Anyone who is required to report or provide information related to drug devices in Pennsylvania needs the Pennsylvania drug device form. This may include healthcare professionals, medical device manufacturers, distributors, or individuals involved in the sale, distribution, or use of drug devices in the state.
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Pennsylvania Drug Device and refers to the reporting requirement for medical devices and drug products in the state of Pennsylvania.
Manufacturers, distributors, and importers of medical devices and drug products are required to file Pennsylvania Drug Device and.
To fill out Pennsylvania Drug Device and, companies must provide details about the medical devices and drug products they manufacture, distribute, or import.
The purpose of Pennsylvania Drug Device and is to ensure the safety and efficacy of medical devices and drug products available in the state.
Information such as product details, manufacturing information, distribution channels, and adverse event reports must be reported on Pennsylvania Drug Device and.
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