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OVERVIEW
OUR SERVICES
INSTRUMENTATION
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ANALYTICAL DEVELOPMENT
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| Capable support of multiple dosage forms |
 Injectables (lyo and non-lyo) |
| Inhalation/Nasal |
| Respiratory |
| Solids, semi-solids, liquids |
| Transdermal |
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Irvine’s fully-compliant cGMP laboratories delivers prompt, reliable development and validation results. In fact, we have developed more than 300 methods in support of a wide range of dosage forms and instrument applications.
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Our scientific depth, innovative approach to seamless project management, and project reports consistently exceed client expectations. In support of pre-clinical, NDA, and ANDA, we start with the application filing date, plan backward to determine fundamental milestones and establish effective timelines to meet your submission date. The process integrates cutting-edge science, embeds quality and safety surveillance, and delivers reliable data submission and post project follow-up.
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At Irvine, our mission is to provide our clients with outsourcing solutions that make their drug development priorities possible.
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