Attachment B CDRH Draft Guidance Cover Sheet

First Page		Document Content
Clinical research Food and Drug Administration Pharmacology Drug discovery Investigational Device Exemption Clinical trial Good Laboratory Practice Pre-clinical development Center for Devices and Radiological Health Pharmaceutical industry Pharmaceutical sciences Research		Attachment B CDRH Draft Guidance Cover Sheet Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 241,10 KB Share Document on Facebook

	Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTS DocID: 1rraL - View Document
	Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices - Draft Guidance for Industry and Food and Drug Administration Staff DocID: 1r7Xt - View Document
	Special circumstances regarding expanded access at Stanford In most circumstances, medical research using investigational drugs, biologics and devices DocID: 1qU9m - View Document
	FAQ’s for Qualifying Clinical Trials What is a qualifying clinical trial? Medicare covers the routine costs of “qualifying clinical trials” as defined below, as well as reasonable and necessary items and services u DocID: 1qPgB - View Document
	Microsoft Word - SOP - Informed Consent - Types and Elements.doc DocID: 1qkZF - View Document