Toggle navigation
Hours
Libraries & Collections
Joyner Library
Laupus Health Sciences Library
Music Library
Digital Collections
Special Collections
Teaching Resources
The ScholarShip Institutional Repository
Country Doctor Museum
Get Help
Toggle navigation
ECU Libraries Catalog
Browse
Call Number
Title
Author
Subject
Series
Course Reserves
More
Search History
New Items
Suggest a Purchase
My Account
Search in
All Fields
Title
Author
Journal Title
Subject
Series
ISBN/ISSN
Publisher
search for
Search
Advanced Search
ECU Libraries Catalog
Toggle facets
Find materials by
Location
Joyner Library
309
Format
Book
309
Electronic
307
Journal
5
Microform
3
Print
1
Publication Date
Publication Date range begin
–
Publication Date range end
Current results range from
1990
to
2010
View distribution
Unknown
1
Collection
Joyner E-Resources
306
Joyner Federal Documents
3
Language
English
309
Genre
Periodicals
5
Electronic records
3
Case studies
1
Statistics
1
Region
United States
217
Search Constraints
Clear Search
You searched for:
Author facet
Center for Biologics Evaluation and Research (U.S.)
Remove constraint Author facet: Center for Biologics Evaluation and Research (U.S.)
« Previous
|
11
-
20
of
309
|
Next »
Sort by Relevance
Relevance
Year DESC
Year ASC
Author
Title
Number of results to display per page
10 per page
10
per page
20
per page
50
per page
100
per page
Search Results
Guidance for industry, FDA staff, and FDA-accredited third parties. Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA).
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : formal meetings between the FDA and sponsors or applicants
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : format and content of proposed risk evaluation and mitigation strategies (REMS), REMS assessments, and proposed REMS modifications
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : integrated summaries of effectiveness and safety : location within the common technical document
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : postmarketing studies and clinical trials, implementation of section 505(o) of the Federal Food, Drug, and Cosmetic Act
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : presenting risk information in prescription drug and medical device promotion
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH region. Annex 2. Test for extractable volume of parenteral preparations general chapter
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH region. Annex 3. Test for particulate contamination : subdivisible particles general chapter
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH region. Annex 4A. Microbiological examination of nonsterile products : microbial enumeration tests general chapter
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
Guidance for industry : Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH region. Annex 4B. Microbiological examination of nonsterile products : tests for specified microorganisms general chapter
2009
Format:
Electronic and Book
✔ Available
Call Number:
Access Content Online
« Previous
Next »
1
2
3
4
5
6
…
30
31