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.

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

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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 M/C consultants

Client List

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

Connect with Us

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