-
FDA OVERSIGHT OF MEDICAL DEVICES: EFFORTS AND DEVELOPMENTS
4,180
博客來
-
CODE OF FEDERAL REGULATIONS TITLE 21 2007 FDA MEDICAL DEVICES
2,888
博客來
-
THE FDA AND WORLDWIDE QUALITY SYSTEM REQUIREMENTS GUIDEBOOK FOR MEDICAL DEVICES
3,392
博客來
-
THE FDA AND WORLDWIDE QUALITY SYSTEM REQUIREMENTS GUIDEBOOK FOR MEDICAL DEVICES
5,092
博客來
-
THE FDA AND WORLDWIDE QUALITY SYSTEM REQUIREMENTS GUIDEBOOK FOR MEDICAL DEVICES
5,500
博客來
-
DEVELOPMENT OF FDA-REGULATED MEDICAL PRODUCTS: PRESCRIPTION DRUGS, BIOLOGICS, AND MEDICAL DEVICES
760
博客來
-
MEDICAL DEVICES AND THE FDA: REGULATION, USER FEES AND TORT CLAIMS
2,356
博客來
-
MEDICAL DEVICE SAFETY: HOW FDA REGULATES THE REPROCESSING OF SUPPOSEDLY SINGLE-USE DEVICES
769
博客來
-
FDA REGULATORY AFFAIRS: A GUIDE FOR PRESCRIPTION DRUGS, MEDICAL DEVICES AND BIOLOGIES
6,458
博客來
-
FDA REGULATORY AFFAIRS: A GUIDE FOR PRESCRIPTION DRUGS, MEDICAL DEVICES, AND BIOLOGICS
13,800
博客來
-
MEDICAL DEVICES AND THE PUBLIC’S HEALTH: THE FDA 510 (K) CLEARANCE PROCESS AT 35 YEARS
3,900
博客來
-
CODE OF FEDERAL REGULATIONS, TITLE 21, PARTS 800-1299 (FOOD AND DRUGS) FDA - MEDICAL DEVICES: REVISED 4/13
2,508
博客來