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Glossary Acronyms for Clinical Research Professionals

- $19.95

Recently updated in 2009 due to popular demand!  

Do you ever wish you had the quickly-evolving terminology of our industry at your fingertips? This easy to use "back-pocket" reference guide helps you to navigate more than 900 key terms and over 500 acronyms that are commonly used in clinical research. This all-new edition has been expanded and includes terms and acronyms for:

  • Clinical Research
  • Pre-Clinical Research
  • Regulatory Submissions
  • Medical Devices
  • Data Management
  • Statistics
  • Pricing and Reimbursement
  • The US, EU, and ICH Regions
 

The 2009 edition is almost twice as long as the previous edition, and includes the terminology you need to know in today's global clinical and regulatory environment. Glossary & Acronyms is an excellent companion to our CFR Reference Guides (for drugs or devices), GCP Question & Answer Reference Guide, and State-by-State Clinical Trial Requirements Reference Guide. This pocket reference guide is ideal for new hire packets, site and management organizations, CRAs, CRCs, sponsors, IRBs, regulatory personnel, QA/QC, research facilities, universities, hospitals, institutions, and more!  Plus, the guides may be customized with your company logo for orders of 100+ books. Great for entire departments, investigator meetings, or tradeshow giveaways! Spiral-Bound Softcover.

For bulk and/or custom cover orders, please call toll-free 1-800-856-2556.




On-Demand GCP Refresher Training 

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Barnett 'Hands-On' In-Person and Web Seminar Workshop Series
Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.


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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 

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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)