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• Guidance : Open Public Meeting : FDA Advisory Committee Meetings
  • 1st Ed. (©2004) from Free Pamphlets (Government Documents)
• Guidance For Human Somatic Cell Therapy And Gene Therapy
  • 1st Ed. (©1998) from Free Books (Government Documents)
• Guidance For Industry : Availability Of Licensed Donor Screening Tests Labeled For Use With Cadaveric Blood Specimens
  • 1st Ed. (©2000) from Free Pamphlets (Government Documents)
• Guidance For Industry : Biological Product Deviation Reporting For Blood And Plasma Establishments
  • 1st Ed. (©2006) from Free Books (Government Documents)
• Guidance For Industry : Biological Product Deviation Reporting For Licensed Manufacturers Of Biological Products Other Than Blood And Blood Components
  • 1st Ed. (©2009) from Free Pamphlets (Government Documents)
• Guidance For Industry : Complementary And Alternative Medicine Products And Their Regulation By The Food And Drug Administration
  • 1st Ed. (©2006) from Free Pamphlets (Government Documents)
• Guidance For Industry : Efficacy Studies To Support Marketing Of Fibrin Sealant Products Manufactured For Commercial Use
  • 1st Ed. (©1999) from Free Pamphlets (Government Documents)
• Guidance For Industry : Errors And Accidents Regarding Saline Dilution Of Samples Used For Viral Marker Testing
  • 1st Ed. (©1998) from Free Pamphlets (Government Documents)
• Guidance For Industry : For Platelet Testing And Evaluation Of Platelet Substitute Products
  • 1st Ed. (©1999) from Free Pamphlets (Government Documents)
• Guidance For Industry : For The Submission Of Chemistry, Manufacturing And Controls And Establishment Description Information For Human Blood And Blood Components Intended For Transfusion Or For Further Manufacture And For The Completion Of The Form FDA 3
  • 1st Ed. (©1999) from Free Books (Government Documents)
• Guidance For Industry : Guidance For Human Somatic Cell Therapy And Gene Therapy
  • 1st Ed. (©1998) from Free Books (Government Documents)
• Guidance For Industry : Guidance On The Labeling Of Certain Uses Of Lecithin Derived From Soy Under Section 403(W) Of The Federal Food, Drug, And Cosmetic Act
  • 1st Ed. (©2006) from Free Books (Government Documents)
• Guidance For Industry : How To Complete The Vaccine Adverse Event Reporting System Form (VAERS-1)
  • 1st Ed. (©1998) from Free Pamphlets (Government Documents)
• Guidance For Industry : Implementation Of Acceptable Full-Length Donor History Questionnaire And Accompanying Materials For Use In Screening Donors Of Blood And Blood Components
  • 1st Ed. (©2006) from Free Pamphlets (Government Documents)
• Guidance For Industry : Informed Consent Recommendations For Source Plasma Donors Participating In Plasmapheresis And Immunization Programs
  • 1st Ed. (©2007) from Free Pamphlets (Government Documents)
• Guidance For Industry : On The Content And Format Of Chemistry, Manufacturing And Controls Information And Establishment Description Information For An Allergenic Extract Or Allergen Patch Test
  • 1st Ed. (©1999) from Free Pamphlets (Government Documents)
• Guidance For Industry : Pharmacogenomic Data Submissions, Companion Guidance
  • 1st Ed. (©2007) from Free Books (Government Documents)
• Guidance For Industry : Questions And Answers Regarding Food Allergens, Including The Food Allergen Labeling And Consumer Protection Act Of 2004 : Final Guidance
  • 4th Ed. (©2006) from Free Books (Government Documents)
• Guidance For Industry : Recommendations For Collecting Red Blood Cells By Automated Apheresis Methods
  • 1st Ed. (©2001) from Free Pamphlets (Government Documents)
• Guidance For Industry : Supplemental Testing And The Notification Of Consignees Of Donor Test Results For Antibody To Hepatitis C Virus (Anti-HCV)
  • 1st Ed. (©1998) from Free Pamphlets (Government Documents)
• Guidance On The Labeling Of Certain Uses Of Lecithin Derived From Soy Under Section 403(W) Of The Federal Food, Drug, And Cosmetic Act
  • 1st Ed. (©2006) from Free Books (Government Documents)