Wherever you are
on the journey,
we make it easy.

For most innovators, their journey begins with a problem to solve, and then an idea. The idea evolves into drawings and specifications, and maybe prototypes are made and tested. But it’s a long way from concept to commercialisation – particularly in highly regulated health markets where product efficacy, safety, quality and product registration requirements are complex.

Let us work with you to develop your end-to-end pathway to market. This is partnership, from conception to prototyping; R&D to product realisation; clinical trial to commercialisation.

null

Where is your product on
its journey to market?

It is important to consider all aspects of design including specific end user requirements and simplicity of manufacture. DEC can assist in the development of product requirement specifications, prototyping using Design for Manufacture principles.
Contact
Scalable, cost-driven manufacturing process design is intricately linked to the future viability of the product. DEC will work with you to develop appropriate process designs and studies to meet your objectives.
Contact
In-process, and final product measurement is at the heart of your product Quality Control. DEC have decades of experience in method development for quantification assays, and measurement. DEC will develop and implement these controls for your product to ensure quality can be tracked and quanitified. This includes testing of raw materials, in-process controls and finished product testing to ensure you receive high quality product that meets specification.
Contact
Our in-house product development and engineering team will work with you to design, specify, procure, install and qualify any new equipment, including production tools required to manufacture/assemble your product.
Contact
Based on your user and product specifications and critical quality attributes, DEC will work with you to develop a Quality Plan, including measurement, stability, documentation and risk assessments.
Contact
Pre-production testing and validation includes manufacturing tool tests, equipment qualification and process and analytical validation. These activities are particularly important for product manufactured and assembled under ISO13485 and cGMP standards. DEC will plan these activities for you as part of our product introduction programme.
Contact
DEC will work with you to transfer into DEC any existing documentation on the product and its manufacturing process. For products made under ISO13485 and cGMP standards this may require documentation to comply with DEC’s processes and procedures.
Contact
DEC has the ability to scale product manufacture with the growth of the product in market. Whether you’re at either end of the product life cycle we can help ensure your product meets your customers’ requirements.
Contact
We often work with companies where the initial demand for the product is low, but the potential is high. DEC can work with you to ensure that scale up, when it arrives, can be handled quickly and efficiently through a range of process studies, and where appropriate, automation of manufacture and assembly processes.
Contact
keyboard_arrow_up