One partner, four connected service lines.
How We Work
Every customer requirement is different: a molecule at feasibility stage, a process ready for scale-up, or a supply relationship that needs a dependable source. Mana Pharma's service model is built to flex across these needs rather than force them into one pathway.
We combine in-house R&D, strategic manufacturing partnerships, contract research and a vetted sourcing network so customers get one point of accountability across development, scale-up, documentation and supply.
Single Point of Accountability
Scientist-Led Technical Discussions
Documentation Ready by Default
Our Services
From early development through to reliable commercial supply, explore how each service line supports your pharmaceutical requirement.
CDMO
01Collaborative development and manufacturing through strategic manufacturing partnerships.
Explore CDMOCRO & Custom Synthesis
02Contract research and custom synthesis shaped around the molecule and its stage.
Explore CROSourcing & Supply
03A network-led approach to sourcing APIs, intermediates, KSMs and specialty materials.
Explore SourcingAPI & Intermediate Development
04Process development with attention to quality, cost, scale and process risk.
Explore DevelopmentCDMO
Mana Pharma supports collaborative development and manufacturing programmes through strategic manufacturing partnerships. We work with customers to align product requirements, process expectations, documentation and manufacturing pathways.
Programme Alignment
Product requirements, process expectations and manufacturing pathways aligned upfront with each customer.
Disciplined Execution
Practical programme management and a disciplined transition from development requirements to manufacturing.
Clear Technical Communication
Scientists remain part of the conversation throughout, keeping technical decisions close to execution.
CRO & Custom Synthesis
Our CRO offering supports partner-specific requirements for APIs, intermediates and KSMs, including custom synthesis and contract research programmes. Each project is shaped around the molecule, development stage, technical objective and expected supply pathway.
Custom Synthesis
Partner-specific synthesis and process work scoped to the molecule and project stage.
Contract Research
Route scouting, process research and analytical work carried out by our in-house R&D team.
Stage-Matched Approach
Project structure shaped around development stage, technical objective and timeline.
Confidential Execution
Project data and commercial context handled with strict partner confidentiality.
Sourcing Services
Mana Pharma provides sourcing support for APIs, intermediates, KSMs and specialty materials through an established network of suppliers. We focus on matching customer requirements with appropriate sources while considering product quality, technical specifications, supply continuity and commercial requirements.
Vetted Supplier Network
An established network assessed for quality systems, capacity and reliability.
Quality-Matched Sourcing
Sources matched to technical specifications and quality expectations for each material.
Supply Continuity
Sourcing decisions weighed against continuity of supply and commercial requirements.
API & Intermediate Development
Our scientific team develops and optimises pharmaceutical processes with attention to quality, cost, time, scalability and process risk. Where appropriate, development programmes can include route selection, alternative reagent evaluation, process optimisation and scale-up planning.
Route Selection
Synthetic routes evaluated for practicality, scalability and commercial relevance.
Reagent Evaluation
Alternative reagents assessed for cost, safety, yield and impurity control.
Process Optimisation
Existing processes improved through focused, targeted optimisation work.
Scale-Up Planning
Development decisions evaluated against plant transfer and reproducibility needs.
Why Mana Pharma
Whichever service line applies to your requirement, the same principles carry through the engagement.
Quality First
Specifications, methods and documentation built with regulated-market expectations in mind.
Scientist-Led
Technical discussions handled directly by scientists, not sales hand-offs.
Documentation Ready
DMFs, method validations and specifications maintained inspection-ready by default.
Have a project in mind?
Whether it is CRO, CDMO, sourcing or process development, our team is ready to discuss the requirement.