Drug Development Consulting
Holistic scientific advice at each stage of drug development
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.
Our team of drug development consultants
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Dr. Vanessa Zann
Senior Drug Development Consultant
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If you have not heard from us in the next 48 hours, do not hesitate to call us on:
UK +44 (0)115 974 9000 / US +1-800-769-3518
Ask questions to our scientific team
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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Scientific PostersA Phase 1, Randomized, Double-Blind, Placebo Controlled, First-in-Human Study to Assess Safety, Tolerability & Pharmacokinetics (PK) of Amilo-5MER in Healthy Volunteers."A Phase 1, Randomized, Double-Blind, Placebo Controlled, First-in-Human Study to Assess Safety, Tolerability & Pharmacokinetics (PK) of Amilo-5MER in Healthy Volunteers." The poster was presented at the Pharmacology 2022 conference and was co-authored with our customer, Galmed Pharmaceuticals
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Scientific PostersBPS 2022 Poster - A Phase 1 Randomized PK Study of Amilo-5MERA Phase 1, Randomized, Double-Blind, Placebo Controlled, First-in-Human Study to Assess Safety, Tolerability & Pharmacokinetics (PK) of Amilo-5MER in Healthy Volunteers
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Scientific PostersAssessment of the Contribution of CYP2D6 to the Elimination of Idalopirdine as well as the Absolute Bioavailability Following Multiple Oral DosingThis study assessed the contribution of CYP2D6 to the metabolization of idalopirdine by comparing pharmacokinetics in CYP2D6 extensive metabolizers (EM) and poor metabolizers (PM) following multiple oral dosing. Comparison of pharmacokinetic (PK) parameters in PMs and EMs may substitute for an interaction study of the effect of CYP2D6 inhibition