Drug Development Consulting
Our Holistic Approach
Our Drug Development Consultants work with you to design and implement successful drug development programs. With industry leading scientific expertise across a range of technical disciplines, we help customers across all stages of development, from candidate selection to commercial launch.
Our consultants have a proven track-record of cutting across industry silos to reduce the time and cost of development. With hands-on development experience across hundreds of drug molecules and product types, we’ll help you avoid critical pitfalls, manage risks and maximise the potential for success.
Leveraging decades of drug development experience
What our consultants do
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Assess each molecule holistically to understand the complex interplay between drug substance, drug product and clinical performance
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Listen to customers, understand goals, interpret data & guide development
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Integrate multiple-development services and build robust development plans
Customer Benefits
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Our consultants pre-emptively identify scientific challenges and mitigate development risks
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Our consultants design drug development strategies that are right first time and eliminating delays
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Our consultants streamline outsourcing, eliminate costly and time-consuming tech transfers and provides consistent scientific direction
Consultancy by stage of development
Candidate Selection - Selecting the right molecules for development
Early Development - Accelerating molecules through to proof-of-concept
Late Development - Accelerating products through to commercial manufacture
From solubility enhancement to complex oral solid dose, from pediatric dosage forms to and injectables, let our experts help you move from discovery into development, from first-in-human to proof-of-concept, and through to late phase and commercial manufacturing.
Resources
Access our resources
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Case StudiesDCS classification of NCE - Case studyUS Biotech wanted to determine the DCS (Developability Classification System) designation for their small molecule. This included project scope and outcomes of the project.
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Case StudiesEndevica Case Study - Peptide Program using Translational PharmaceuticsEndevica Bio is developing TCMCB07 as a novel synthetic peptide product for the potential treatment of cachexia. Read how they leveraged the Quotient Sciences Translational Pharmaceutics platform for this program.
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Case StudiesEnsysce Biosciences Case StudyRequest a copy of our latest case study with Ensysce Biosciences about how our integrated strategies helped them achieve their regulatory milestones faster for PF614-MPAR, an Extended Release product.
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Info SheetDrug-Drug Interaction (DDI) StudiesAssessing how your drug interacts with other drugs in vivo is a critical step in the drug development process and is essential in ensuring safe and efficacious drug delivery. This assessment is known as a drug-drug interaction (DDI) study and is a regulatory requirement for submissions of investigational new drugs (INDs). Learn more about Quotient Sciences' offering for DDI studies.