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Quotient’s Andy Lewis appointed as Secretary of Controlled Release Society
Quotient’s Andy Lewis appointed as Secretary of Controlled Release Society
Quotient is your answer.
Quotient is your answer.
We are dedicated to accelerating the development of new drugs for patients around the world. We provide CRO and CDMO services including formulation development, clinical pharmacology trials, and clinical and commercial manufacturing services to the pharmaceutical and biotech industry. These services are provided either individually or as an integrated service offering via our Translational Pharmaceutics® platform.
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How do I accelerate my molecule to proof-of-concept?
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Quotient is your answer.
How do I accelerate my molecule to proof-of-concept?
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How do I optimize my formulation?
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Quotient is your answer.
How do I optimize my formulation?
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How do I optimize and scale up my manufacturing process for the later stages of development and commercial launch?
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Quotient is your answer.
How do I optimize and scale up my manufacturing process for the later stages of development and commercial launch?
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How do I efficiently plan and execute my regulatory clinical pharmacology studies?
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Quotient is your answer.
How do I efficiently plan and execute my regulatory clinical pharmacology studies?
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How do I develop age-appropriate drug products for pediatric populations?
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Quotient is your answer.
How do I develop age-appropriate drug products for pediatric populations?
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Fact Sheet
Formulation Development
From preclinical and first-in-human (FIH) dosage forms to optimization of your drug products for late stage development, we work with you to develop the most appropriate formulation.
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Webinar
From candidate selection through to proof-of-concept
Building a robust understanding of your API characteristics matched against your development programme goals, supports the efficient transition of drug products from candidate selection through to proof-of-concept. Starting @ 4pm (BST-UK), 11pm (ET), 8am (PT) and 6pm (BST-UK), 1pm (ET), 10am (PT)