Expert bioanalytical and drug development solutions

The help you need, when you need it, from the experts who know how to get it done.


Bring us into your drug development project early and we will minimize your regulatory risk


We routinely perform regulatory risk assessments

  • CROs identified as having high risk issues
  • CROs having performed or preparing to perform your drug development projects
  • The Bioanalytical portion of your submission documentation


  • Bioanalytical Support for Toxicology
  • Bioanalytical Support for Clinical Studies
  • Review Regulatory Submissions (IND/NDA)

Our network of consultants also include

  • Toxicology
  • Quality Assurance
  • EU Clinical Development Services

When the number of projects exceeds your critical mass; when your staff doesn’t have the experience to run the programs and get the approvals or when you discover your submission is at risk you need; call on the Experts at Stubbs and Hensel.

In the highly competitive biopharmaceutical marketplace, the need to diversify, innovate, and globalize is paramount.  The pressure and cost to get new drug solutions to market is greater than ever.  It can stretch your resources to the breaking point or push your staff beyond their capabilities, putting your investment and even your company at risk.  In this highly specialized world, you need experts who have years of experience partnering with the FDA and understand all aspects of regulated bioanalysis.  A partner who can help you navigate the complex road of drug development and regulatory submissions.  You need the experts at Stubbs & Hensel. Learn more.

BA Project Management

We assure that your bioanalytical data have been generated with the least regulatory risk possible, on time and on budget.

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BA Forensic Auditing

The help you need, when you need it, from the experts who know how to get the job done.

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Drug Development

Stubbs & Hensel can recruit the right people to manage your drug development project.

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