Manufacturing

As a cGMP manufacturer, Irvine Labs adheres to the strictest pharmaceutical and supplement manufacturing processes. We manufacture APIs and end products for research and commercial use in humans and veterinary use.

Contract Manufacturing

Irvine Labs offers contract product development and manufacturing services providing specialty pharmaceutical solutions with botanical drug medicine and DEA scheduled active pharmaceutical ingredients.

Good Agricultural Practices (GAP) Cultivation

Irvine Labs has over 12 years of experience in botanical drug cultivation.

We apply Good Agricultural Practices (GAP) to cultivation, which is a set of standards for the safe and sustainable production of crops and livestock. It aims to help farm owners maximize yields and optimize business operations while also minimizing production costs and environmental impact. 

GAP compliance audits are voluntary and can be audited by the U.S. Department of Agriculture (USDA) to ensure compliance with Food and Drug Administration (FDA) guidelines.

Collaborative Manufacturing Research

The research and science team at Irvine Labs works with our partners to continuously improve botanical extraction and manufacturing processes.  

Clinical Trial Materials

Irvine Labs specializes in industry leading botanical drug manufacturing for Phase I, Phase II and Phase III clinical trial materials.