Image of a gloved hand holding a vial of powder Image of a gloved hand holding a vial of powder

Development Stages

From Discovery to Delivery: Full Spectrum Support Across the Drug Development Lifecycle

We provide seamless, scientifically driven support across every stage of development, uniting chemistry, biology, analytical, process and regulatory expertise to help bring your molecule from concept to clinic.

The Partnership Promise

Drug development isn’t a series of isolated projects, it’s a continuum where success at each stage depends on the quality of the one before it. That’s why we build long-term partnerships that align science, strategy, and execution from the earliest route design to post-approval lifecycle management.

Our integrated model connects discovery chemistry and biology with analytical development, process development and regulatory strategy in one continuous flow. With stage-aligned experts and proactive communication, we make sure you stay in control of your molecule’s journey.

Our Services
Development Stages
Design, Make, Test, Select
Our Design-Make-Test-Select (DMTS) workflow unites chemistry, bioscience, and analytics under one framework to deliver fully integrated drug discovery services across small molecules, peptides, oligonucleotides, and hybrid modalities.
IND/IMPD enabling
We help you develop a cohesive, regulatory-ready strategy that aligns CMC, nonclinical, and analytical development to meet global submission standards.
Phase I clinical development
We bridge the gap between discovery and first-in-human, ensuring your process, material, and data are ready for GMP manufacturing.
Phase II clinical development
We help you strengthen your manufacturing and analytical foundations, building the process understanding, data integrity, and technical control needed to move to late-stage development and commercial readiness.
Phase III process development and control
We help you define, demonstrate, and document control, aligning science, data, and strategy to achieve process validation and regulatory approval.
Post approval support
We help you maintain validated processes, strengthen control strategies, and adapt efficiently to post-approval changes, ensuring continued compliance.
Design, Make, Test, Select

Our Design-Make-Test-Select (DMTS) workflow unites chemistry, bioscience, and analytics under one framework to deliver fully integrated drug discovery services across small molecules, peptides, oligonucleotides, and hybrid modalities.

Explore Design, Make, Test, Select

IND/IMPD enabling

We help you develop a cohesive, regulatory-ready strategy that aligns CMC, nonclinical, and analytical development to meet global submission standards.

Explore IND/IMPD enabling

Phase I clinical development

We bridge the gap between discovery and first-in-human, ensuring your process, material, and data are ready for GMP manufacturing.

Explore Phase I Development

Phase II clinical development

We help you strengthen your manufacturing and analytical foundations, building the process understanding, data integrity, and technical control needed to move to late-stage development and commercial readiness.

Explore Phase II Development

Phase III process development and control

We help you define, demonstrate, and document control, aligning science, data, and strategy to achieve process validation and regulatory approval.

Explore Phase III Development

Post approval support

We help you maintain validated processes, strengthen control strategies, and adapt efficiently to post-approval changes, ensuring continued compliance.

Explore Post Approval Support

Support across the entire drug development pipeline

From route design and scale-up to analytical control and technology transfer, our integrated services help our partners deliver life changing medicines to patients faster.

Why Stage-Aligned Support Matters

A generic CRO/CDMO model doesn’t reflect the realities of modern development. Scientific requirements, regulatory risks, and operational complexity shift at every milestone. By aligning our support to your stage, we help you:
Avoid premature or unnecessary spend
Minimise downstream rework and repeat analysis
Generate decision-enabling data at the right time
Navigate complex regulatory expectations with clarity
1 / 1
“True development success comes from the continuity of a single scientific vision carried through every phase. We provide that alignment, so your data, strategy, and delivery move as one.”
Ross Burn
CEO, CatSci

What You Can Achieve

Faster Progression to Clinic and Market
Reduce transition times between phases through integrated planning and proactive coordination
Stronger Regulatory Confidence
Present cohesive data packages and narratives that meet global regulatory expectations the first time
Optimized Resource Utilization
Eliminate duplication across functions, conserving time, budget, and materials
Enhanced Data Integrity
Maintain a single scientific thread from discovery through to approval, ensuring traceability and credibility
Scalable Global Expansion
Build flexible frameworks for multi-region filings, extensions, and lifecycle growth
Enduring Partnership and Trust
Work with a single, accountable team that remains aligned with your goals from start to finish

Book a Consultation

Speak directly with our scientists about your development challenges and explore how we can support your programme.