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Num
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Titles (1-50 of 334)
Year
Entries
367 Found
1
Guidance for industry
5
2
Guidance for industry and clinical investigators [electronic resource] : the use of clinical holds f
2004
1
3
Guidance for industry and FDA [electronic resource] : current good manufacturing practice for combin
2004
1
4
Guidance for industry and FDA review staff [electronic resource] : collection of platelets by automa
2007
1
5
Guidance for industry and FDA staff
12
6
Guidance for industry and FDA staff [electronic resource] : application user fees for combination pr
2005
1
7
Guidance for industry and FDA staff [electronic resource] : class II special controls guidance docum
2007
1
8
Guidance for industry and FDA staff [electronic resource] : commercially distributed analyte specifi
2007
1
9
Guidance for industry and FDA staff [electronic resource] : devices used to process human cells, tis
2007
1
10
Guidance for industry and FDA staff [electronic resource] : early development considerations for inn
2006
1
11
Guidance for industry and FDA staff [electronic resource] : expedited review of premarket submission
2008
1
12
Guidance for industry and FDA staff [electronic resource] : how to write a request for designation (
2005
1
13
Guidance for industry and FDA staff [electronic resource] : interactive review for medical device su
2008
1
14
Guidance for industry and for FDA staff [electronic resource] : enforcement priorities for single-us
2000
1
15
Guidance for industry and review staff [electronic resource] : labeling for human prescription drug
2009
1
16
Guidance for industry and review staff [electronic resource] : nonclinical safety evaluation of refo
2008
1
17
Guidance for industry and review staff [electronic resource] : recommended approaches to integration
2006
1
18
Guidance for industry and staff [electronic resource] : minimal manipulation of structural tissue ju
2006
1
19
Guidance for industry and staff [electronic resource] : resolution of disputes concerning payment or
2004
1
20
Guidance for industry : complementary and alternative medicine products and their regulation by the
2006
1
21
Guidance for industry, dairy farms, bulk milk transporters, bulk milk transfer stations and fluid mi
2003
1
22
Guidance for industry - dosage delivery devices for OTC liquid drug products [electronic resource].
2011
1
23
Guidance for industry - dosage delivery devices for over the counter liquid drug products
2011
1
24
Guidance for industry [electronic resource].
2002
1
25
Guidance for industry [electronic resource] : 21 CFR, part 11, electronic records : electronic signa
2002
1
26
Guidance for industry [electronic resource] : 21 CFR part 11, electronic records, electronic signatu
2001
1
27
Guidance for industry [electronic resource] : 180-day exclusivity when multiple ANDAs are submitted
2003
1
28
Guidance for industry [electronic resource] : 180-day generic drug exclusivity under the Hatch-Waxma
1998
1
29
Guidance for industry [electronic resource] : acceptance of foreign clinical studies
2001
1
30
Guidance for industry [electronic resource] : acute bacterial otitis media, developing drugs for tre
2008
1
31
Guidance for industry [electronic resource] : acute bacterial sinusitis, developing drugs for treatm
2007
1
32
Guidance for industry [electronic resource] : addendum to E2C clinical safety data management : per
2004
1
33
Guidance for industry [electronic resource] : adequate and appropriate donor screening for hepatitis
2007
1
34
Guidance for industry [electronic resource] : adverse reactions section of labeling for human prescr
2006
1
35
Guidance for industry [electronic resource] : advisory committee meetings : preparation and public a
2008
1
36
Guidance for industry [electronic resource] : advisory committees : implementing Section 120 of the
1998
1
37
Guidance for industry [electronic resource] : aerosol steroid product safety information in prescrip
1997
1
38
Guidance for industry [electronic resource] : alternate source of the active pharmaceutical ingredie
2000
1
39
Guidance for industry [electronic resource] : amendment (donor deferral for transfusion in France si
2006
1
40
Guidance for industry [electronic resource] : an acceptable circular of information for the use of h
2003
1
41
Guidance for industry [electronic resource] : ANDAs, impurities in drug products.
2005
1
42
Guidance for industry [electronic resource] : ANDAs, impurities in drug substances.
2009
1
43
Guidance for industry [electronic resource] : ANDAs, pharmaceutical solid polymorphism, chemistry, m
2007
1
44
Guidance for industry [electronic resource] : animal models : essential elements to address efficacy
2009
1
45
Guidance for industry [electronic resource] : antiviral product development, conducting and submitti
2006
1
46
Guidance for industry [electronic resource] : assessing donor suitability and blood and blood produc
2005
1
47
Guidance for industry [electronic resource] : availability of licensed donor screening tests labeled
2000
1
48
Guidance for industry [electronic resource] : available therapy.
2004
1
49
Guidance for industry [electronic resource] : bar code label requirements, questions and answers.
2006
1
50
Guidance for industry [electronic resource] : bioanalytical method validation.
2001
1
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