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Barnett International Announces New SOP Development and Optimization Courses
February 21, 2012
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February 20, 2012
Barnett Educational Services Announces Buy One, Get One Free DVD Holiday Sale!
December 15, 2011
Hamrell Appointed Editor of Barnett International’s Good Clinical Practice: A Question & Answer Guide
November 16, 2011
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September 29, 2011
Barnett Educational Services Announces Buy One, Get One Free DVD Sale!
June 6, 2011

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FOR IMMEDIATE RELEASE

Barnett International Announces New SOP Development and Optimization Courses

Needham, MA, February 21, 2012 — Barnett International announced today the launch of an ongoing series of web-based courses focused on SOP development, optimization and standardization. The goal of the series is to help attendees create user-friendly SOPs that continuously support standards for quality and validity of data, as required by the regulations, while also providing value to their users.

Key topic areas include:

• Procedural Document System: Organized Development
• SOP on SOPs and Procedural Document Templates
• Five Key Strategic Steps for Developing Global SOPs
• Preparing for SOP Inspection: An Auditor’s Perspective
• Implementation of Procedural Documents

Taught by Barnett’s lead SOP development subject matter experts, the courses cover a range of learning objectives including how different types of procedural documents can be used to improve quality, compliance and efficiency, how to perform a cross-functional process inventory, how to identify key points about the SOP on SOPs and how this document affects other procedural documents. Also included is a methodology for developing effective global SOPs, as well as the FDA’s new expectations for SOPs from Sponsors/CROS and Clinical Investigators (with an update on IRB requirements).

“We are very excited about this new series, and in particular, the emphasis on recent case studies concerning issues in SOP documentation and implementation practices.  Through the interactive features built into the courses, participants will have the opportunity to discuss lessons learned common pitfalls to avoid,” said Naila Ganatra, Barnett’s General Manager.

Barnett’s new courses are available as web-based training courses which can also be brought to your site, providing a high degree of flexibility for learners. To view Barnett International’s complete catalog of training courses, download the 2012 catalog at http://www.healthtech.com/EducationalServices/br+dl.aspx.  For our full portfolio of training opportunities, including industry publications, on-site training programs, eLearning programs, and other consulting opportunities, please visit: www.BarnettInternational.com

About Barnett International: Founded in 1979, Barnett International is widely recognized for its superior consulting services and its targeted education and training programs. Barnett helps clients get the most out of their research and development dollars by managing change effectively, improving organizational performance, and enhancing staff knowledge. The Barnett approach is a unique combination of strategy development and practical, hands-on implementation. The "Barnett Difference" is evident in our deep understanding of the clinical research process and in the rapid and tangible performance improvements we deliver.

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On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.


GCP for Investigators
 

Barnett’s scenario-based eLearning course is designed with the busy Principal Investigator in mind.  Based on real-life scenarios encountered by investigative site teams, this highly focused 7-module GCP training is designed to ensure comprehensive understanding of the key components of GCP.

For more details on this scenario-based eGCP program for investigators please click here. 


BARNETT CATALOG The Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

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Blended Curriculum Path for the CRA, CRC, and Project Manager

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Live SeminarLIVE SEMINARS

Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


Web SeminarWEB SEMINARS

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)