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Access to experienced analytical scientists and state-of-the-art equipment is critical to the success of your drug development program. At Quotient Sciences, we pride ourselves on providing the best analytical support, delivering candidate screening, drug product analysis and phase-appropriate method development and validation.
Our material science experts have a proven track record in rapidly characterizing API properties in order to support the selection of lead drug product formats for pre-clinical and clinical evaluation:
We understand your analytical objectives throughout the drug development process and work with you to ensure that appropriate methodologies are available at all stages. We offer support and trouble-shooting capabilities including:
Our qualified and experienced microbiologists pride themselves on applying their knowledge and skills to ensure that pharmaceutical
drug substances and drug products are safe and meet today’s rigorous quality specifications and regulatory standards.
We also work closely with our own clinics and other clinical research units to provide a rapid results service within 24 to 48 hours to support extemporaneous preparations.
For more information about our microbial capabiltiies, click here.
We have extensive experience in the testing of drug products from preclinical development through to commercial drug products including:
We offer a full stability storage and testing service that satisfies ICH guidelines for the stability assessment of your drug products. Our fully validated, controlled and monitored stability storage includes: