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Quotient Sciences

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uuid0004w4a

Namestring
Quotient Sciences
Legal namestring
Quotient Sciences
Company typeenum
Private
Founded yearint
1990
Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersNottingham, United Kingdom
HQ citystring
Nottingham
HQ countrystring
United Kingdom
HQ regionstring
Europe
Markets served

Serves global market

Offices6 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
contract pharmaceutical development, drug product manufacturing, clinical pharmacology services, formulation development services, early phase clinical trials
Industry4 codes
PRIMARYHLAGAOAK
CMC, Process Development & Tech Transfer Staffing FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
SECONDARYHLAGAHAL
GMP Scale-Up, Tech Transfer & Process Validation (PPQ)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/API & Small-Molecule Development/Manufacturing Services
SECONDARYHLAGAOAH
Clinical Trial Supply, Logistics & Vendor Management FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
SECONDARYHLAGAOAL
Manufacturing, MSAT & Operations Staffing (API/Biologics/Cell & Gene)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
NAICS code4 codes
  • Scientific Research and Development Services5417
  • Research and Development in the Physical, Engineering, and Life Sciences54171
  • Pharmaceutical Preparation Manufacturing325412
  • Other Scientific and Technical Consulting Services541690
SIC code2 codes
  • Services-Commercial Physical & Biological Research8731
  • Services-Medical Laboratories8071
Product category
Contract Pharmaceutical Development and Manufacturing (CRDMO)
Social media profiles2 records
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1CRDMO Contract Services
TypeProfessional Services
Description

Integrated contract services spanning drug substance manufacturing, drug product development, and clinical trial services. Revenue generated through project-based contracts with pharmaceutical and biotech companies.

2Clinical Development Services
TypeProfessional Services
Description

Phase I clinical trials, clinical pharmacology studies, and bioanalysis services billed through project contracts.

3Commercial Manufacturing
TypeProfessional Services
Description

Manufacturing services for approved products including commercial supply agreements such as the Ipsen partnership for Sohonos (palovarotene).

Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales
Pricing details1 tier
1Custom project-based pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Contract services priced based on project scope, duration, and complexity. No standard pricing tiers publicly available.

GTM typeB2B
B2B
Offering typeServices
Services
Brand1 of 2 records shown
1Translational Pharmaceutics®
Description

Integrated drug development platform combining formulation development, GMP manufacturing, and clinical testing under single project management for accelerated timelines.

quotientsciences.com
+1 more record
Core offering1 text field

Quotient Sciences is a CRDMO (Contract Research, Development, and Manufacturing Organization) providing integrated pharmaceutical development services. Its flagship Translational Pharmaceutics platform combines formulation development, cGMP manufacturing, and clinical testing under a single project management team. Supporting services include Phase I early clinical development, formulation development, human ADME studies, commercial drug product manufacturing, and data sciences.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 1,300+ Phase I studies delivered
+2 more records
Product overview1 text field

Quotient Sciences is a CRDMO (Contract Research, Development, and Manufacturing Organization) providing integrated pharmaceutical development services. The core offering is the Translational Pharmaceutics® platform, which uniquely integrates formulation development, GMP manufacturing, and clinical testing under single project management. Supporting services include Early Clinical Development (Phase I trials), Formulation Development, Human ADME Studies (via Synthesis-to-Clinic®), Pharmacy Compounding, Data Sciences, and Commercial Manufacturing. AI capabilities are being integrated through the ANDROMEDA machine learning platform partnership with Intrepid Labs for formulation optimization.

Product and service1 record
1Translational Pharmaceutics
Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership6 partners
Strategic tierCoreTypeTechnology or IntegrationAnnounced on2024-01-01
Description

Multi-year strategic partnership to integrate Intrepid Labs' ANDROMEDA AI platform into Quotient Sciences' formulation development processes. This collaboration enhances AI-guided formulation development capabilities, enabling accelerated optimization of drug formulations using machine learning algorithms.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Strategic partnership providing integrated clinical development pathways combining Quotient Sciences' Translational Pharmaceutics and manufacturing capabilities with Lindus Health's clinical trial expertise. Aims to streamline drug development from preclinical through Phase II studies.

Strategic tierCoreTypeChannel Partner/ Reseller/ Distributor
Description

Strategic partnership delivering integrated early phase clinical trial solutions. Combines Biorasi's global clinical operations expertise with Quotient Sciences' formulation development and manufacturing capabilities for seamless early-stage development programs.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Commercial manufacturing partnership for Sohonos (palovarotene), a treatment for fibrodysplasia ossificans progressiva. Quotient Sciences manufactures and supplies commercial product for the approved therapy.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Participation in the Horizon Europe-funded ETERNAL project focused on advanced pharmaceutical manufacturing technologies. Collaboration with IRIS Technology Solutions and other partners on process innovation.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Joint venture focused on mRNA therapeutics development and manufacturing. Combines Quotient Sciences' pharmaceutical development expertise with CPI's process innovation capabilities for next-generation nucleic acid medicines.

Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Medpace is a mid-sized clinical CRO focused on full-service clinical development for small to mid-sized biopharma. Comparable to Quotient Sciences on the early clinical development and Phase I service overlap, with similar mid-tier positioning relative to mega-CROs, though Medpace lacks drug product manufacturing capabilities.

TypeBroad incumbent
Description

ICON plc is a leading global CRO providing Phase I-IV clinical development, bioanalytical, and consulting services. Compares to Quotient Sciences on early clinical development and Phase I clinical pharmacology services, though ICON's portfolio extends well beyond early-phase into late-stage and post-approval studies.

TypeBroad incumbent
Description

Lonza is a Swiss-based global CDMO providing drug substance and drug product services across small molecules, biologics, and cell/gene therapy. Compares to Quotient on the contract manufacturing and formulation development side, though it operates at far greater scale with a much wider service portfolio including biologics.

TypeBroad incumbent
Description

IQVIA is the world's largest CRO offering clinical trial services, laboratory services, and real-world evidence. Comparable to Quotient Sciences on Phase I clinical pharmacology and bioanalysis services, though IQVIA's scope spans the full clinical lifecycle and operates at vastly larger scale.

TypeDirect peer
Description

Recipharm is a European CDMO offering drug substance and drug product development and manufacturing services. Compares to Quotient Sciences on formulation development and contract manufacturing capabilities, with similar mid-tier positioning, though Recipharm's portfolio is more weighted toward commercial manufacturing.

TypeBroad incumbent
Description

WuXi AppTec is a Chinese-headquartered global CRDMO providing drug discovery, development, and manufacturing services. Comparable to Quotient Sciences on integrated CRDMO offerings, formulation development, and clinical services, though it operates at substantially larger scale with broader geographic reach across Asia and beyond.

TypeDirect peer
Description

Worldwide Clinical Trials is a mid-sized CRO specializing in early-phase clinical development, bioanalysis, and Phase II/III studies. Direct peer to Quotient Sciences on Phase I clinical pharmacology and early-phase clinical services, with similar mid-market positioning focused on complex and rare disease programs.

TypeBroad incumbent
Description

Catalent (now owned by Novo Holdings) is a global CDMO with extensive formulation development, clinical supply, and commercial manufacturing services. Compares to Quotient Sciences across drug product development and manufacturing, but operates at significantly larger scale with a broader service portfolio across biologics, softgel, and oral technologies.

TypeBroad incumbent
Description

Thermo Fisher Scientific's PPD CDMO business provides end-to-end drug substance, drug product, and clinical development services following its acquisition of Patheon. Comparable to Quotient Sciences on integrated CDMO offerings, though at substantially larger scale with broader scientific and operational capabilities.

TypeBroad incumbent
Description

Charles River Laboratories offers preclinical, clinical, and manufacturing services to pharma/biotech. Comparable to Quotient on the early-phase clinical and CDMO side, with overlapping capabilities in drug substance and drug product development, though substantially larger in scale and broader in scientific scope.

Market position
Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers12 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI capability3 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles12 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries3 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance5 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors1 record

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A4 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Quotient Sciences

Contract Pharmaceutical Development and Manufacturing (CRDMO)quotientsciences.com

Quotient Sciences firmographics

Firmographics
Name
Quotient Sciences
Legal name
Quotient Sciences
Website
https://quotientsciences.com
Company type
Private
Founded year
1990
Operating status
Operating
Headcount range
1,001–5,000 employees
Ownership category
akta.pro rank

Quotient Sciences industry classification

Industry
Product category
Contract Pharmaceutical Development and Manufacturing (CRDMO)
NAICS
Scientific Research and Development Services (5417), Research and Development in the Physical, Engineering, and Life Sciences (54171), Pharmaceutical Preparation Manufacturing (325412), Other Scientific and Technical Consulting Services (541690)
SIC
Services-Commercial Physical & Biological Research (8731), Services-Medical Laboratories (8071)
akta.pro industry
PRIMARYHLAGAOAK
CMC, Process Development & Tech Transfer Staffing FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
SECONDARYHLAGAHAL
GMP Scale-Up, Tech Transfer & Process Validation (PPQ)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/API & Small-Molecule Development/Manufacturing Services
SECONDARYHLAGAOAH
Clinical Trial Supply, Logistics & Vendor Management FSP
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)
SECONDARYHLAGAOAL
Manufacturing, MSAT & Operations Staffing (API/Biologics/Cell & Gene)
Healthcare & Life Sciences/Life Science Tools & Services (CRO/CDMO/Lab Services)/Scientific Staffing & Functional Service Providers (FSP)

Keywords

  • Contract pharmaceutical development
  • Drug product manufacturing
  • Clinical pharmacology services
  • Formulation development services
  • Early phase clinical trials

Where Quotient Sciences is headquartered

Location

Headquarters

HQ city
Nottingham
HQ country
United Kingdom
HQ region
Europe

Offices6 records

Markets served

Quotient Sciences business model

Business model
GTM type
B2B
Offering type
Services
Cost components
Personnel, Operations, Infrastructure, Technology or R&D, Supply Chain, Marketing or Sales

Revenue model

  1. CRDMO Contract Services: Integrated contract services spanning drug substance manufacturing, drug product development, and clinical trial services. Revenue generated through project-based contracts with pharmaceutical and biotech companies.
  2. Clinical Development Services: Phase I clinical trials, clinical pharmacology studies, and bioanalysis services billed through project contracts.
  3. Commercial Manufacturing: Manufacturing services for approved products including commercial supply agreements such as the Ipsen partnership for Sohonos (palovarotene).

Pricing tiers

ModelBillingPrice
OtherMulti-year contractCustom project-based pricing

Go-to-market motion3 records

Distribution channels3 records

Marketing channels6 records

Quotient Sciences product offering

Product offering

Core offering

Quotient Sciences is a CRDMO (Contract Research, Development, and Manufacturing Organization) providing integrated pharmaceutical development services. Its flagship Translational Pharmaceutics platform combines formulation development, cGMP manufacturing, and clinical testing under a single project management team. Supporting services include Phase I early clinical development, formulation development, human ADME studies, commercial drug product manufacturing, and data sciences.

Product overview

Quotient Sciences is a CRDMO (Contract Research, Development, and Manufacturing Organization) providing integrated pharmaceutical development services. The core offering is the Translational Pharmaceutics® platform, which uniquely integrates formulation development, GMP manufacturing, and clinical testing under single project management. Supporting services include Early Clinical Development (Phase I trials), Formulation Development, Human ADME Studies (via Synthesis-to-Clinic®), Pharmacy Compounding, Data Sciences, and Commercial Manufacturing. AI capabilities are being integrated through the ANDROMEDA machine learning platform partnership with Intrepid Labs for formulation optimization.

Differentiator

Problem solved

Functional benefit

Brands

  • Translational Pharmaceutics®: Integrated drug development platform combining formulation development, GMP manufacturing, and clinical testing under single project management for accelerated timelines.
  • Synthesis-to-Clinic®

Products and services

  • Translational Pharmaceutics

Quantifiable outcome

  • 1,300+ Phase I studies delivered
  • +2 more outcomes

Companies that use Quotient Sciences

Customer profile

Named customers12 records

Segments3 records

Ideal customer profiles3 records

Quotient Sciences technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability3 records

Feature3 records

Quotient Sciences partnerships and signals

Strategic signal

Partnerships

Six partnerships are on record, tiered core and minor.

  • Intrepid LabscoreTechnology or Integration · 1 January 2024Multi-year strategic partnership to integrate Intrepid Labs' ANDROMEDA AI platform into Quotient Sciences' formulation development processes. This collaboration enhances AI-guided formulation development capabilities, enabling accelerated optimization of drug formulations using machine learning algorithms.
  • Lindus HealthcoreChannel Partner/ Reseller/ DistributorStrategic partnership providing integrated clinical development pathways combining Quotient Sciences' Translational Pharmaceutics and manufacturing capabilities with Lindus Health's clinical trial expertise. Aims to streamline drug development from preclinical through Phase II studies.
  • BiorasicoreChannel Partner/ Reseller/ DistributorStrategic partnership delivering integrated early phase clinical trial solutions. Combines Biorasi's global clinical operations expertise with Quotient Sciences' formulation development and manufacturing capabilities for seamless early-stage development programs.
  • IpsencoreStrategic or Co-development PartnerCommercial manufacturing partnership for Sohonos (palovarotene), a treatment for fibrodysplasia ossificans progressiva. Quotient Sciences manufactures and supplies commercial product for the approved therapy.
  • IRIS Technology SolutionsminorStrategic or Co-development PartnerParticipation in the Horizon Europe-funded ETERNAL project focused on advanced pharmaceutical manufacturing technologies. Collaboration with IRIS Technology Solutions and other partners on process innovation.
  • CPI (Centre of Process Innovation)minorStrategic or Co-development PartnerJoint venture focused on mRNA therapeutics development and manufacturing. Combines Quotient Sciences' pharmaceutical development expertise with CPI's process innovation capabilities for next-generation nucleic acid medicines.

Scale indicators8 records

Recent moves9 records

Expansion highlights6 records

Quotient Sciences competitors and assessment

Company assessment

Direct peers

  • Medpace: Medpace is a mid-sized clinical CRO focused on full-service clinical development for small to mid-sized biopharma. Comparable to Quotient Sciences on the early clinical development and Phase I service overlap, with similar mid-tier positioning relative to mega-CROs, though Medpace lacks drug product manufacturing capabilities.
  • Recipharm: Recipharm is a European CDMO offering drug substance and drug product development and manufacturing services. Compares to Quotient Sciences on formulation development and contract manufacturing capabilities, with similar mid-tier positioning, though Recipharm's portfolio is more weighted toward commercial manufacturing.
  • Worldwide Clinical Trials: Worldwide Clinical Trials is a mid-sized CRO specializing in early-phase clinical development, bioanalysis, and Phase II/III studies. Direct peer to Quotient Sciences on Phase I clinical pharmacology and early-phase clinical services, with similar mid-market positioning focused on complex and rare disease programs.

Broad incumbents

  • ICON plc: ICON plc is a leading global CRO providing Phase I-IV clinical development, bioanalytical, and consulting services. Compares to Quotient Sciences on early clinical development and Phase I clinical pharmacology services, though ICON's portfolio extends well beyond early-phase into late-stage and post-approval studies.
  • Lonza Group: Lonza is a Swiss-based global CDMO providing drug substance and drug product services across small molecules, biologics, and cell/gene therapy. Compares to Quotient on the contract manufacturing and formulation development side, though it operates at far greater scale with a much wider service portfolio including biologics.
  • IQVIA: IQVIA is the world's largest CRO offering clinical trial services, laboratory services, and real-world evidence. Comparable to Quotient Sciences on Phase I clinical pharmacology and bioanalysis services, though IQVIA's scope spans the full clinical lifecycle and operates at vastly larger scale.
  • WuXi AppTec: WuXi AppTec is a Chinese-headquartered global CRDMO providing drug discovery, development, and manufacturing services. Comparable to Quotient Sciences on integrated CRDMO offerings, formulation development, and clinical services, though it operates at substantially larger scale with broader geographic reach across Asia and beyond.
  • Catalent: Catalent (now owned by Novo Holdings) is a global CDMO with extensive formulation development, clinical supply, and commercial manufacturing services. Compares to Quotient Sciences across drug product development and manufacturing, but operates at significantly larger scale with a broader service portfolio across biologics, softgel, and oral technologies.
  • Thermo Fisher Scientific (CDMO services): Thermo Fisher Scientific's PPD CDMO business provides end-to-end drug substance, drug product, and clinical development services following its acquisition of Patheon. Comparable to Quotient Sciences on integrated CDMO offerings, though at substantially larger scale with broader scientific and operational capabilities.
  • Charles River Laboratories: Charles River Laboratories offers preclinical, clinical, and manufacturing services to pharma/biotech. Comparable to Quotient on the early-phase clinical and CDMO side, with overlapping capabilities in drug substance and drug product development, though substantially larger in scale and broader in scientific scope.

Market position

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Quotient Sciences social profiles

Digital presence

Quotient Sciences compliance and trust

Trust signal

Compliance5 records

Quotient Sciences financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Quotient Sciences leadership team

Management profile

Number of profiles

Profiles12 records

Quotient Sciences subsidiaries and ownership

Company hierarchy

Subsidiaries3 records

Quotient Sciences funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors1 record

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Quotient Sciences M&A and investment

M&A and investment

M&A4 records

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Quotient Sciences

What does Quotient Sciences do?

Quotient Sciences is a CRDMO (Contract Research, Development, and Manufacturing Organization) providing integrated pharmaceutical development services. Its flagship Translational Pharmaceutics platform combines formulation development, cGMP manufacturing, and clinical testing under a single project management team. Supporting services include Phase I early clinical development, formulation development, human ADME studies, commercial drug product manufacturing, and data sciences.

Is Quotient Sciences a public or private company?

Quotient Sciences is a private company. It is classified as private equity controlled and is currently operating.

When was Quotient Sciences founded?

Quotient Sciences was founded in 1990. It employs 1,001 to 5,000 people.

Where is Quotient Sciences based?

Quotient Sciences is headquartered in Nottingham, United Kingdom, in the Europe region.

How does Quotient Sciences make money?

Three revenue lines are on record. CRDMO Contract Services are the primary driver. The others are clinical Development Services and commercial Manufacturing.

Who are Quotient Sciences's main competitors?

Direct peers on record are Medpace, Recipharm and Worldwide Clinical Trials. Broad incumbents are ICON plc, Lonza Group, IQVIA, WuXi AppTec, Catalent, Thermo Fisher Scientific (CDMO services) and Charles River Laboratories.

Does Quotient Sciences have an API?

No public API is recorded for Quotient Sciences.

What industry is Quotient Sciences in?

Quotient Sciences's product category is Contract Pharmaceutical Development and Manufacturing (CRDMO). Its primary akta.pro industry code is HLAGAOAK, CMC, Process Development & Tech Transfer Staffing FSP, with a secondary code of HLAGAHAL, GMP Scale-Up, Tech Transfer & Process Validation (PPQ). Its NAICS code is 5417 and its SIC code is 8731.

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Live signals
PR NewswireQuotient Sciences and Acesion Pharma Announce Collaboration on AI-Enhanced Formulation Development to Advance Atrial Fibrillation PipelineQuotient Sciences and Acesion Pharma announced a collaboration using Quotient's AI-enhanced formulation development within its Translational Pharmaceutics platform to support Acesion's atrial fibrillation pipeline. The solution applies machine learning and Bayesian optimization to prioritize drug products, aiming to shorten development timelines. Acesion is developing SK ion channel inhibitors, with AP30663 in clinical trials.Digital Health NewsQuotient Sciences, Acesion Pharma Partner on AI-Driven Drug DevelopmentQuotient Sciences and Acesion Pharma partnered to apply AI-enhanced formulation development to Acesion's atrial fibrillation pipeline. The collaboration uses active machine learning and Bayesian optimization to assess formulation data, aiming to accelerate development decisions and shorten clinical testing timelines.News-MedicalQuotient Sciences proprietary AI-enhanced solution optimizes formulation in clinical studyQuotient Sciences reported interim results from a clinical study where its AI algorithm selected modified-release formulation compositions and doses, reaching a preset pharmacokinetic target within three dosing periods. The algorithm learned the relationship between tablet composition and human pharmacokinetics quickly, after screening one-third fewer formulations than conventional methods. Dosing continues, with full data expected toward the end of the year.PR NewswireQuotient Sciences Proprietary AI-Enhanced Solution Optimizes Formulation in Clinical StudyQuotient Sciences reported interim results from a clinical study where an AI algorithm selected modified-release tablet compositions and doses, reaching a preset pharmacokinetic target within three dosing periods. The algorithm learned the relationship between formulation and human performance quickly, and dosing continues with full data expected by year-end.PR NewswireQuotient Sciences Proprietary AI-Enhanced Solution Optimizes Formulation in Clinical StudyQuotient Sciences reported interim results from a clinical study where an AI algorithm selected modified-release tablet compositions and doses, reaching a preset pharmacokinetic target within three dosing periods. The algorithm learned the relationship between formulation and human performance quickly, and dosing continues with full data expected by year-end.PharmTechEvolving Approaches to Taste MaskingThe article reviews evolving taste-masking technologies for oral drug products, highlighting advanced strategies such as reverse-enteric polymers, melt-granulation, and lipid encapsulation to improve patient compliance. Experts from Quotient Sciences and BASF Pharma Solutions discuss the technical challenges of masking bitter APIs in various dosage forms, including liquids and high-drug-loading solids. These developments aim to balance effective taste suppression with maintained pharmacokinetic performance and manufacturing efficiency.PharmTechPharma Fundamentals: Utilizing AI in Drug DevelopmentThe article discusses the increasing use of artificial intelligence (AI) in drug development within the pharmaceutical industry, highlighting its role in shortening timelines and optimizing the drug discovery process. It details regulatory principles established by the FDA and EMA, and presents a real-world example of a strategic partnership between Quotient Sciences and Intrepid Labs to advance AI-guided formulation development. The article emphasizes the importance of high-quality data, regulatory engagement, and maintaining human oversight for successful AI integration.Scientist LivePhase I Clinical Trial for AI-Designed Drug FormulationQuotient Sciences has initiated a Phase I clinical study at its UK facility to evaluate an AI-designed oral solid dose formulation, following approval from the MHRA. The trial, which uses Intrepid Labs' machine learning algorithm, aims to validate AI's potential to accelerate drug formulation development and improve clinical decision-making. The company claims this is the first reported case of an AI-designed formulation entering clinical evaluation, marking a milestone in AI-enabled pharmaceutical development.PR NewswireQuotient Sciences Advances AI-Designed Drug Product into Clinical DevelopmentQuotient Sciences has initiated a Phase I clinical study at its UK facility evaluating a novel oral drug formulation designed using artificial intelligence, following approval from the Medicines and Healthcare products Regulatory Agency (MHRA). The company claims this represents the first reported case of an AI-designed formulation being evaluated in clinical development, with the study leveraging Intrepid Labs' machine learning algorithm for formulation design and optimization. Quotient Sciences plans to share further data and updates as it expands its AI-enabled capabilities across formulation development and clinical workflows.PR NewswireQuotient Sciences Advances AI-Designed Drug Product into Clinical DevelopmentQuotient Sciences initiated a Phase I clinical study of an AI-designed oral solid dose formulation in healthy volunteers, approved by the MHRA. The study aims to validate AI in drug product development, marking the first reported case of an AI-designed formulation in clinical trials. The company expects further updates over the coming months.