May 19, 2024
Data standards support the robust organization, analysis, and reporting of clinical trials and many regulatory...
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Apr 19, 2024
If you’re contemplating a Functional Service Provision (FSP) model to enhance your biometric team, understanding...
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Apr 19, 2024
Choosing to supplement your internal biometrics team via Functional Service Provision (FSP) offers numerous benefits,...
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Apr 19, 2024
Pharma and biotech companies often face the challenge of needing additional biometrics support, whether due...
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Mar 18, 2024
Bioforum and Dren Bio (“Dren”) joined forces to focus on Dren’s first clinical trial evaluating DR-01 in patients...
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Dec 05, 2023
Selecting the right Contract Research Organization (CRO) is a critical decision for any pharmaceutical, biotech,...
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Dec 05, 2023
In today’s evolving clinical research and drug development landscape, with more data sources and technology...
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Sep 11, 2023
Audit trails are a regulatory requirement. How to take an RBQM approach. Audit trails have...
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Jul 24, 2023
For many sponsors of clinical trials, particularly the smaller pharmaceutical, biotech, and medical device companies,...
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Jul 10, 2023
By Dionne Crafford In the first of two posts on lean medical writing, we were...
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