Specific development

As a fully integrated group, SGH Medical Pharma designs and produces custom-made medical devices. We take charge of your idea from the design stage, based on your specifications and requirements, right through to delivery of the final product. With our injection know-how and strong industrial capabilities, we have the potential to become your contract manufacturer of choice to help you succeed.

Our development methods are governed by a strict and rigorous quality monitoring process, based on several stages:

A team dedicated to handling your concepts and projects

  • From needs analysis to intellectual property management, our R&D department contributes its expertise and creativity at every stage of project development.
  • Once the specifications have been drawn up, the concept is brought to life in several phases: feasibility checks, 3D drawings, non-functional modelling and prototyping in the factory or using Fused Deposition Modeling (FDM). We master both Design-to-cost and Design-to-value approaches, while ensuring eco-design where relevant.
  • Our industrialisation team then scales up production to ensure that manufacture, assembly and packaging meet your requirements and fit your product perfectly. We ensure that all your quality, dimensional and functional concerns are taken into account, from the most basic to the most technical parts, while scrupulously following product and process risk assessment protocols to eliminate any hazards.
  • All our projects are managed by a project manager, supported by a multi-disciplinary team. And because we are aware that each project is unique and involves different regulatory constraints and quality tools, a development quality manager is entirely dedicated to supporting your project from the initial idea right through to delivery of the finished product, working closely with the project manager.
  • By managing the development of your product from start to finish, we provide you with a turnkey medical device as well as the technical documentation required for CE marking. We write all your technical documentation ready for registration and keep it up to date with regulatory changes and/or changes to the device.

In the current global context of pressure on the supply of plastic raw materials, our specialist purchasing team ensures sustainable supplies as part of our business continuity plan.