Creating Multiple Forest Plots in SAS Using Macros and ODS Graphics
A guide to generating Forest Plots in SAS with macros, GTL, and SGPLOT to streamline outputs for clinical trials and subgroup analysis.
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Regulatory Medical Writing: Everything You Need to Know
Explore regulatory medical writing: its role in drug development, essential documents, key skills, and best practices for compliance.
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DO Loops in SAS: Iterative, Conditional, and PROC DS2 Multithreading
Learn SAS DO loops from Base to PROC DS2: iterative, list-based, conditional, nested loops, and multithreading for faster data processing.
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An Introduction To Biostatistics In Clinical Trials
Understand how biostatistics drives reliable results in clinical trials, ensuring data integrity, patient safety, and regulatory confidence.
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Human Gene Therapy Clinical Trials for Hemophilia A & B
Discover the latest hemophilia gene therapy clinical trials, FDA-approved treatments, key challenges, and future directions in durable, single-dose care.
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FDA's Project Optimus: What You Need to Know
Explore the FDA's Project Optimus, an initiative aimed at optimising oncology drug dosing to enhance efficacy and minimise toxicity in cancer treatments.
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What is Biometrics in Clinical Trials?
Discover how biometrics in clinical trials drives personalised medicine, from genetic insights to tailored treatments.
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The Role of Clinical Trial Data Visualisation in Modern Drug Development
Explore how clinical trial data visualisation enhances oversight, accelerates timelines, and drives smarter decisions.
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First Steps in Laboratory Dataset Handling: From SAS to R
Streamline lab data workflows with tips for SAS and R, covering everything from standardisation, macros, and regulatory readiness.
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What is a Late Phase CRO? Understanding Their Role in Drug Development
Learn what a late-phase CRO is, their role in Phase IIIb/IV trials, and how they support real-world evidence and long-term safety monitoring.
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Understanding CDISC Standards in Clinical Research: A Complete Guide
Discover how CDISC standards support reliable clinical trial data, real-world evidence, and harmonised global submissions.
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SAS Proc Transpose In Clinical Trial Programming
Explore how SAS PROC TRANSPOSE is used in clinical trial programming to reshape data for analysis and reporting.
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