Getting a new medical device product approved by regulators is complex and often challenging. What do the statistics tell us about the approval process for a new medical device? What can we learn, and how can you ensure your path to regulatory approval is as smooth as possible? The following five statistics about the medical … 5 Medical Device Regulatory Approval Statistics You Need to Know
With the development of new products, innovations, and technologies, analysts are predicting healthy growth in the medical device industry over the coming years. What are the main trends in MedTech as we go into 2023? More specifically, what are the trends in minimally invasive medical device design? Prioritising Ease of Use, Clinical Outcomes, and Patient … Trends in Minimally Invasive Medical Device Design
By Conor Thompson The manufacturing techniques used in the production of your medical device product will have a significant impact on everything from quality to manufacturability to costs. Overmolding is one manufacturing technique that can have a significant and positive influence on all these factors. In this blog, we’ll explain how overmolding works, how it … How Overmolding Can Improve Your Medical Device Product
Medical device regulations are complex. They are also regularly updated and refined. So, rather than being a fixed set of rules, they constantly evolve. Therefore, it’s essential to have access to medical device regulatory experience and expertise during the application process. Third-party regulatory support can be beneficial for companies of any size, but it is … 4 Tips for Choosing a Medical Device Regulatory Consultant
Your medical device start-up has fantastic potential, but it’s essential to make the right decisions today to maximise its value in the future and make it attractive to investors and/or potential buyers. That means finding the right partners to progress your idea. Running a start-up medical device company is an exciting but often very busy … How Arrotek Adds Value to Your Medical Device Start-Up Company
By Richard McLoughlin Bringing a new medical device product to market is an intensive and extensive process, so it’s important you get the right support. The best approach is to work with a partner that offers a complete service offering, with end-to-end support from the concept development stage through to full-scale manufacturing. At Arrotek, we … Medical Device Design Services – Support from Concept to Full-Scale Production
Arrotek has been named as one of two finalists for the MedTech Company of the Year Award at the Irish MedTech Awards 2022. The Irish MedTech Awards are run by the Irish MedTech Association, Enterprise Ireland, and IDA Ireland. The MedTech Company of the Year Award is one of nine awards that will be announced … Arrotek Shortlisted for MedTech Company of the Year 2022
Arrotek Medical has opened a new office in Massachusetts, USA. The office is part of our strategic growth plans and will enhance the service we offer to our growing client base in the US and Canada. Richard McLoughlin, Sales and Marketing Manager at Arrotek, said: “The United States has been an important market for us … Arrotek Medical Opens US Office
By Paula Johnson While fine needle aspiration (FNA) and fine needle biopsy (FNB) are common procedures for the diagnosis of cancer, there is no specific device option that is the best choice in all situations. In fact, there is a large range of design and feature options available in both the FNA and FNB categories … Choosing the Right Fine Needle Aspiration or Fine Needle Biopsy Device
Design transfer is a phrase that describes the activities and processes that introduce a medical device design to production. Effective design transfer is required by regulators but it also keeps manufacturing costs under control and ensures production milestones and deadlines are met. Furthermore, effective design transfer can reduce time to market and improve product quality. What … Three-Phase Design Transfer Process to Prepare a Design for Manufacturing
