Board of Administration Agenda Template 3

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Date: 2013-08-21 14:12:53 Drugs Pharmaceuticals policy Clinical pharmacology Biosimilar Biotechnology Biologic Generic drug Food and Drug Administration Prescription medication Pharmacology Pharmaceutical sciences Clinical research		Board of Administration Agenda Template 3 Add to Reading List Source URL: www.gphaonline.org Download Document from Source Website File Size: 65,65 KB Share Document on Facebook

	Commited to Biologic Innovation DocID: 1tUBq - View Document
	Special Authorization Criteria for Biologic Drugs For each disease category specified below, the biologic drugs listed will only be considered for reimbursement if the patient has failed an adequate trial or experienced DocID: 1tOXv - View Document
	ASX ANNOUNCEMENT 10 February 2014 Cynata Partners With Leading Biologic Product Manufacturer Cynata Therapeutics Ltd (ASX:CYP), announced today that it has signed a manufacturing agreement DocID: 1tf2X - View Document
	Stakeholder Meeting on PDUFA VI Reauthorization September 28, 2015, 1:30 PM – 3.05 PM FDA White Oak Campus, Silver Spring, MD Purpose To discuss the current status of the human drug and biologic review programs, review DocID: 1t2jx - View Document
	Council Report AVMA Council on Biologic and Therapeutic Agents’ report on cat and dog vaccines Donald J. Klingborg, DVM; David R. Hustead, DVM; Elizabeth A. Curry-Galvin, DVM; Nigel R. Gumley, DVM, DABVP; Steven C. Hen DocID: 1s94L - View Document