ISO 7 cleanroom filling
Process architecture for filling and packaging operations requiring an ISO 7 environment as defined by the project.
Contract development and manufacturing
One team, from feasibility to industrial batch.
We integrate formulation science, process engineering and regulatory judgement to reduce uncertainty and build products that can be manufactured consistently.
01—04
Development governed by technical decisions
- 01
Define the scope
Intended use, professional user, markets, format, actives, volume and regulatory pathway.
- 02
Design the formula
Raw-material selection, prototypes and decisions on stability, compatibility and user experience.
- 03
Verify and transfer
Controls, product–pack compatibility, critical parameters and transfer to industrial conditions.
- 04
Manufacture with traceability
Production, filling, identification, document review and release within the agreed scope.
A connected development chain
- Feasibility assessment
- Development and reformulation
- Technical prototyping
- Scale-up and transfer
- Product–pack compatibility
- Filling and packaging
- Documentation support
- Batch follow-up
Specialist services
Three areas working as one project
Choose the closest starting point; final scope is confirmed after reviewing formula, format, market and scale.
Purified-water PW loop
Control of the purified-water system, points of use, sanitisation and monitoring of critical parameters.
Nitrogen-purge filling
Protective-atmosphere filling design for oxygen-sensitive formulas, subject to compatibility and validation.
CDMO model
Contract manufacturing with one technical responsibility
Our model connects formula, process, components, controls, documentation and industrial planning.
Emerging brands
A structured route from concept to product without an in-house industrial team.
Laboratories and distributors
Complementary capacity for new categories, formats or transfers.
Clinical teams
Turn professional experience into a repeatable, usable and documented product.
International brands
Development aligned from the outset with target markets and a verifiable supply chain.
FAQ
Contract-manufacturing questions
What can a CDMO project include?
Feasibility, formula development or transfer, prototyping, scale-up, packaging selection, manufacturing, filling and documentation support.
Can you transfer an existing formula?
Yes, after reviewing composition, method, raw materials, specifications, stability, packaging and usage rights.
How are timing and cost calculated?
After scope, complexity, testing, components, volume and markets have been defined.
Etternity Dermal
You need a partner, not disconnected suppliers
Bring development and manufacturing into one traceable technical conversation.