2009 CFR/ICH GCP Guide x185  

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CFR ICH GCP Reference Guide 2009 (Spiral Bound)

- $13.95

Our 2009 CFR/ICH GCP Reference Guide contains:  

  • FDA Code of Federal Regulations, Good Clinical Practice parts 11, 50, 54, 56, 312, & 314.
  • Good Laboratory Practice Part 58
  • ICH Guidelines Good Clinical Practice (E6) and Clinical Safety Data Management (E2A)
  • The European Union Clinical Trials Directive and The European Union Good Clinical Practice Directive.
 

New Feature for 2009!"Editor's Notes" that alert you to changes to the Federal Register that will take effect after the April 1, 2009 publication date.

Updated annually in April.

Standard orders of 100+ books are only $9.95 per book!
This Guide can also be customized with your company logo for orders of 100+ books. Call for details.
4"x7" spiral bound soft cover pocket guide.
Perfect binding also available.

Device-Specific CFR Guide also available.
 




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Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


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10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  


PublicationsPUBLICATIONS

2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)