Manufacturing
Manufacturing
As a cGMP manufacturer, Irvine Labs adheres to the strictest pharmaceutical manufacturing processes. We manufacture APIs and end products for research and commercial use in humans and veterinary use.
Schedule 1 Contract Manufacturing
Irvine Labs is also a pharmaceutical contract manufacturing organization. We focus on contract development and manufacturing services providing specialty pharmaceutical solutions with botanical drug medicine and Schedule 1 active pharmaceutical ingredients.
Good Agricultural Practices (GAP) Cultivation
Irvine Labs has over 10 years of experience in botanical cultivation, including cannabis – both hemp and marijuana.
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 Schedule 1 and botanical-based Phase I, Phase II and Phase III clinical trial materials.
