Research & Planning
We understand the evolving environment in which medical and pharma companies operate, whether it be emerging technology trends, shifts to patient preferences, or the changing pattern of diseases.
Our experts have a breadth of experience in enabling businesses to de-risk decision-making or the product development process, from feasibility studies for new concepts, working to quality management standards, to confidential technical due diligence reviews for possible partnerships or acquisitions.

Feasibility Studies

Project Management
To ensure the efficient and effective delivery of projects, we have embedded project management tools within our design process. This ensures the design team can closely monitor schedules, provide regular updates and ultimately ensure on time delivery of the project.
Our lean structure and process enables us to remain flexible through the development and adapt quickly to project changes.

Due Diligence Support

Market Analysis

Technology Scouting & Landscaping

Quality Management
Through a global portfolio of customers, we’re experienced in working with a variety of regulations and FDA guidelines. We work to ISO 13485, ISO 62366 and IEC 60601 standards.
Our services encompass full project support. This includes the creation of all necessary technical documentation to regulatory submissions. We will create DHF and DMR documentation for risk management regulation and compliance. We can create and manage these documents in our own templates, or work within your systems.
View our medical product research and planning capabilities in action: