This year Arrotek took part in the Spirit of Christmas Gift Appeal by buying a gift for a resident of Nazareth House nursing home in Sligo. It was a small offering, but very much appreciated by the residents of Nazareth house and brightened up what can be a lonely time of year for some of … Arrotek’s Spirit of Christmas!!
Arrotek were delighted to sponsor a prize for the Innisfree Athletics Club 5K Christmas Cracker last month. Congratulations to all involved!
As we have covered in a previous blog, risk management is essential when designing and developing a new medical device product. An important part of this process involves creating and maintaining a risk management plan. Before going any further, it’s helpful to define risk management. What is risk management? Risk management is not the act … Medical Device Risk Management Plan – What You Need to Know
Risk management is an essential part of the medical device product design process. It ensures the safety of patients, users, and operators so it’s no surprise that risk management is a regulatory requirement. Risk management is also essential to the medical and commercial success of the new product you plan to develop. In terms of … An Overview of Risk Management in Medical Device Product Design
We’re delighted to announce that Arrotek has had zero turnover of permanent staff in over 12 months! This is a fantastic achievement for our company – it is a testament to you all to have a group of employees who continually strive and are committed to the continued success of Arrotek. Without you, Arrotek would … Arrotek has had zero turnover of permanent staff in over 12 months
Design verification and design validation are essential parts of the medical device product development process. Sometimes referred to as V&V, it’s important to understand what both terms mean and how they differ if you are about to embark on a medical device product development project. This is because V&V can take more time than necessary … Medical Device Design Verification and Design Validation – What They Are and Why They Are Important
We’re absolutely delighted to sponsor Sligo Rovers F.C. U15s on their trip to Germany. It was great to meet the squad in person and we wish them the best of luck on the trip! Arrotek have supported Sligo Rovers over the years to help the club with their continued success.
Arrotek will be one of the 70 indigenous Irish MedTech companies exhibiting at Med in Ireland next week. Med in Ireland is a key event for the MedTech industry both in Ireland and in Europe. Taking place once every two years, it is led by Enterprise Ireland to highlight innovation in Ireland’s MedTech sector and … Arrotek Exhibiting Med in Ireland Event Next Week
In a previous article, we outlined the importance of identifying and documenting user needs when designing a new medical device product. In that article, we looked at the two objectives you must achieve when documenting user needs: This sounds straightforward enough but when you go through it in practice, the process can be quite tricky, … Documenting User Needs – Key Questions You Need to Answer
You have an idea for a new medical device – this is the starting point for all new product development projects. Where the project goes from there, however, the costs involved, and the timeline depends on a range of factors. Examples include the complexity of the product, availability of funding, regulatory issues, medical trials, and … How Design Changes Impact Medical Device Product Development Costs and Time to Market
