Services
Capabilities across the pharmaceutical lifecycle
Twelve capability areas, each with typical activities, technologies, example projects and a clear statement of what we lead and what qualified partners perform.
Science & development
Pharmaceutical Research & Development
Structured research and development support that moves a product idea through pre-formulation, formulation, analytical and process work to …
Product & Formulation Development
From prototype to a robust, scalable formulation: dosage-form design, optimisation and the process knowledge that makes a product manufactu…
CRO / Contract Research
Research and development studies coordinated with contract research organisations, with DGXPComplianceLab managing scope, data and document…
Contract Laboratory Services
Analytical testing, method work and stability programmes arranged with contract laboratories, with clear lines between what we do and what …
Manufacturing
External Manufacturing
Identifying, evaluating and coordinating qualified external manufacturers so your product is made where the technical, quality and regulato…
CMO / CDMO Services
Contract manufacturing and contract development-and-manufacturing support, coordinated through qualified partner organisations.
Technology & digital
Technology Design, Build, Test & Verify
Engineering pharmaceutical technology the way it will be inspected: requirements first, designed and built to them, then tested and verifie…
Pharmaceutical Digital Transformation
Converting paper-based and fragmented pharmaceutical processes into controlled, connected digital workflows that stay compliant.
Pharmaceutical Software Solutions
Software designed around pharmaceutical workflows — requirements, workflow design, validation and documentation included from the start.
AI & compliance
AI Across the Pharmaceutical Lifecycle
Practical AI where it helps pharmaceutical work — research, development, manufacturing, quality, regulatory, laboratory and supply chain — …
AI Governance & AI Validation
AI is not implemented simply because it is available. In pharmaceutical work it needs an intended use, a risk assessment, validation and li…
Regulatory, Quality & Documentation Practices
GxP compliance, validation and documentation practices that make pharmaceutical work traceable, reviewable and inspection-ready.
How capabilities are delivered
DGXP-led Assessment, planning, coordination, documentation, software, validation and AI governance led by our team.
Partner-coordinated Manufacturing, laboratory testing and study conduct performed by qualified partner organisations, coordinated by us.
Project capability is subject to technical assessment and partner availability.
Our project execution model
Every engagement follows the same eight steps, scaled to the size and risk of the project.
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01
Understand
Understand business and technical requirements.
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02
Assess
Assess scientific, technical, regulatory and operational requirements.
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03
Design
Design the appropriate solution.
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04
Identify
Identify appropriate internal and external capabilities and partners.
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05
Execute
Coordinate and execute the project.
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06
Verify
Test, verify, qualify or validate where applicable.
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07
Document
Create technical, quality and regulatory documentation.
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08
Improve
Monitor, optimise and continuously improve.
Have a research, manufacturing, technology or digital requirement?
Tell us what you need. We will discuss scope, the capabilities involved and how the project could be executed.