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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

Feasibility Studies

It’s important to check the practicality of a concept. We apply a process that establishes the overall project objectives and confirms the product requirements, creating concepts or even prototype tooling for technical assessment and commercial feasibility.
Project management gantt chart for medical project on laptop screen

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.

Technical due diligence report positioned on a tabletop

Due Diligence Support

If you want to understand the detailed technical offering of a potential partnership or acquisition, we can perform a confidential technical review on your behalf, while also maintaining the confidence of the disclosing party.
people in meeting talking about product trends to represent market analysis

Market Analysis

Work with our experienced team to uncover valuable insights and opportunities by analysing existing and future products, markets and trends.
people talking at a conference with a lung display with advanced technologies

Technology Scouting & Landscaping

As technologies continue to emerge, we can look at the technology spaces that matter to you. This enables strategic decisions on your product pipeline to provide a competitive edge in both the short and long term.
Shore Group LRQA ISO 13485 certificate of approval

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: