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Drug Substance, API Development, Solubility Enhancement
Preclinical Technology Screening
2 October 2024
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Translational Pharmaceutics, Formulation Development
Accelerating Development of 505(B)(2) Product
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Translational Pharmaceutics, Drug Product Optimization, Real-Time Manufacturing, First-in-Human
Translational Pharmaceutics® Fact Sheet
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Drug Product Optimization, Commercial Manufacturing, Clinical Trial Manufacturing, Real-Time Manufacturing, Formulation Development
Global Formulation Development and Manufacturing Capabilities
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Commercial Manufacturing, Clinical Trial Manufacturing
Quotient Sciences High Potency Handling Info Sheet
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Spray Drying, Drug Product Optimization, Formulation Development
Spray Drying Services
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Clinical Trial Manufacturing, Formulation Development
Quotient Sciences Aseptic Development & Manufacturing Capabilities
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Translational Pharmaceutics, Clinical Trial Manufacturing, Real-Time Manufacturing, Formulation Development
Integrated Programs: Early Development
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Translational Pharmaceutics, Human ADME, Pediatrics, Regulatory Affairs, High Potency Handling, Drug Substance, Drug Product, Bioanalysis, Microbiology, Analytical Services, Radiosynthesis, Isotopic Labeling, Solubility Enhancement, Modified Release, Spray Drying, Drug Product Optimization, Commercial Manufacturing, Clinical Trial Manufacturing, Real-Time Manufacturing, Gamma Scintigraphy, Formulation Development, Clinical Pharmacology, Oncology, First-in-Human
Quotient Sciences Corporate Brochure 2022
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Bioanalysis
Bioanalytical Services
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Translational Pharmaceutics, Commercial Manufacturing, Clinical Trial Manufacturing, Real-Time Manufacturing, Formulation Development, First-in-Human
Project Management at Quotient Sciences
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Spray Drying, Drug Product Optimization, Formulation Development, Oncology
Formulation Strategies for Poorly Soluble Molecules
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Pediatrics, Drug Product Optimization, Formulation Development
Pediatric Development
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Translational Pharmaceutics, Clinical Pharmacology, First-in-Human
First-in-Human to Proof-of-Concept
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Commercial Manufacturing, Pediatrics, Oncology
Quotient Sciences' Commercial Manufacturing Capabilities
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Modified Release, Formulation Development
Modified-Release Formulation Strategies
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Pediatrics, Clinical Trial Manufacturing, Real-Time Manufacturing, Formulation Development, Clinical Pharmacology
Global Clinical Trial Supplies
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Pediatrics, Formulation Development
Developing a Poorly Tasting Drug Substance into a Palatable Dosage Form
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Clinical Pharmacology, Modelling & Simulation
PBPK Modelling & Simulation
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Human ADME, Spray Drying
Pre-formulation and Material Sciences
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Human ADME
Drug-Drug Interaction (DDI) Studies
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Human ADME, Radiosynthesis, Clinical Pharmacology
Human ADME Capabilities
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Human ADME, Isotopic Labeling
Isotope Labelling
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Translational Pharmaceutics
Integrated Pharmacy Compounding and GMP Manufacturing Fact Sheet
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Formulation Development
Formulation Development
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Clinical Trial Manufacturing
Clinical Trial Manufacturing
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Quotient Sciences and Charles River Collaboration
Quotient Sciences' Collaboration with Charles River
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Drug Substance
Drug Substance Synthesis and Manufacturing
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Formulation Development
Peptide Development Strategies
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Analytical Services
Stability Capabilities
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Clinical Pharmacology
Clinical Pharmacology Info Sheet
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Formulation Development
Inhaled Product Development
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Analytical Services
Microbiology Services
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