MCCULLEY/CUPPAN INC.
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About Us

Since 1994, McCulley/Cuppan has been working with a diverse range of life sciences companies to improve the quality of their mission-critical documents and enhance organizational work practices. 

McCulley/Cuppan provides a full range of consulting, training, and writing support services. We help companies, teams, and individuals:
  • Plan and execute document design strategies. 
  • Identify messages and issues that development and regulatory documents must effectively address.
  • Design and produce high-quality regulatory documents that help advance development projects in a timely manner.
  • Develop effective standards to ensure document usability and readability.
  • Manage the representation of individual and team knowledge in documents.
  • Understand the elements required for
    ​best-of-class technical and regulatory writing.
  • Apply best practices to the document review process.
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Learn More:

Gregory has shared articles on LinkedIn with insight into our experience and services:

Writing Teams Need to Apply More Time Thinking About User Experience
​Thinking About Audience: The Situation of Use
​Constructing Scientific Argument in Regulatory Briefing Documents

By the Numbers

  • 10,000+: pharma & biotech professionals trained
  • 60+: client companies and institutions worldwide

Team Work

  • Decades of Experience
  • Numerous project teams in all major therapeutic areas supported by MC consultants

Client List

  • ​Bristol-Myers Squibb
  • Johns Hopkins University
  • Novartis
  • Complete Client List

Connect with Us

  • Writing in the Life Sciences blog
  • LinkedIn
  • Twitter
  • Contact Us

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© COPYRIGHT 2022. ALL RIGHTS RESERVED.
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  • Home
  • Books
  • Consulting
    • Strategic Review
    • Assessment Services
  • Training
    • Skills Development Workshops
  • About
    • Experience
    • Client List
    • Blog
    • Document Standards
  • Contact