WHY US
We will lead you through our Product Design Method to deliver results.
PROVEN DESIGN PROCESS
Tensen follows a stage gated Product Design Method to reduce the risk and iterations required to deliver your product. Our five-step gated roadmap is a proven methodology that reduces scope creep and churn helping us maintain budget and timelines.
Product development is not for the weak at heart, but with Tensen you have a partner on the journey ahead. We aim to cut the fat out, maximizing your ROI.
We pride ourselves on establishing timelines and budgets that can be met.
Our unique position in the product design services market is our ability to perform non-linear creative activities in a timely manner that can be budgeted against. Our experience provides insight to identifying early on in the project the potential trial and error sections of the development path that can push timelines and budgets out of scope. Together we identify the risks, and plan accordingly. We don’t suggest that we are able to identify all risks in the planning stage, but with our gated Product Design Method we are able to address issues as they arise in a controlled manner.
Tensen is set apart from the rest by its ability to understand your business goals and objectives, translating them into the products you hired us to design.
DESIGN DRIVEN RESULTS
Tensen is committed to delivering quality product design that meets our clients technical and performance requirements time and time again.
We create lasting brand equity through real business value to our clients.
Offering a diverse skill set of innovative product design and manufacturing know-how for over a decade, we are focused on working with your budget and time requirements, to deliver the results you need. Through qualitative analysis we are able to orchestrate and customize to our clients diverse requirements. We build an enduring relationship with our clients to see the product from inception through delivery.
We are used to designing Medical products for our clients that are ISO 13485 certified. We are compliant to the design standards necessary for your Design History File, DHF + Device Master Record, DMR. When designing a medical device we focus on risk management and design controls during the product development. Root cause analysis, DFMEA, PFMEA, CAPA and the 5 Why’s are just some of the processes we implement to ensure compliance with the regulatory bodies during FDA and Health Canada submissions.