Here at Red Medtech we are passionate about patient care, innovative medical technology and equally supporting all sizes of organisations from micro start-ups and university spin-outs, large global blue-chip companies, to Small and Medium Enterprises (SMEs).
Our expertise in project leadership, product development and compliance includes design, engineering, production, quality and regulatory - bringing a wealth of knowledge and experience across a wide range of technologies.
We have successfully supported a variety of medical device, biopharmaceutical, healthcare technology and life sciences customers. Let's discuss how we can help you:
We have delivered a number of successful medtech projects for some great companies and worked with some wonderful people. Rather than simply take our word for it, we collated some feedback of their experiences partnering with Red Medtech, so we can share these with you.
Turns out they've had some awfully nice things to say and so here is a sample of those testimonials and recommendations.
And have you seen our extensive experience across different healthcare technologies? Check out some of the the medical devices we have worked on here:
“Red Medtech, with Laurie Rowe, was an invaluable partner for Made for Movement (MFM) post-Brexit. They provided clarity on UKCA requirements, helping us navigate local regulations in the UK and Ireland.
Their expertise also shed light on our Technical File’s compliance with the UK MDR. We highly recommend Red Medtech as your regulatory consultant!”
"I would not hesitate in recommending Laurie for technical acumen, attention to detail, excellent regulatory compliance, technical documented diligence at the required development rate. "
"Laurie is a highly competent engineer and I would recommend her as a medical device specialist! "
"From my experience with Laurie she has been a successful project manager on a number of key projects, taking the lead in several. Laurie has worked with cross functional teams to define the product definition and functionality on a number of electromechanical projects."
"Laurie has successfully undertaken the Regulatory Managers role covering the MMD and MDR requirements to drive the electromechanical product definition for a new state of the art medical surgical device."
"When I recruited Laurie it was her passion, honesty and straight forward attitude that really got my attention. Working with her she showed high level abilities in driving to answers, innovating, creativity and dealing with diversity & variability. "
"I have had the pleasure of previously working with Laurie within a couple of organisations now and she has always been the consummate professional. She has an abundance of both knowledge and practical application experience, which she uses to great effect in a collaborative and positive manner. She is also very personable and humble within the workplace."
"Knowledgeable in her field and never scared to provide an educated opinion, I had absolute comfort in letting Laurie run with work knowing she would deliver more and better results each time. "
"I had the pleasure of working with Laurie at Biomet. Her work was always calm and professional, and she was a pleasure to work with. "
"I find Laurie easy to work with and she easily fits in with any team, bringing a professional approach and a lot of knowledge across a diverse range of products. Including, regulatory management, product definition, development, customer usability, risk management and manufacturing. "
"I have known and worked with Laurie Rowe for over 4 years and found her to be enthusiastic and professional in any task she has undertaken. Laurie is a team player and works well in any diverse product development environment, achieving targets at the same time getting the best out of cross functional team members."
"I would not hesitate to recruit her onto a team of mine for the positive impact I know she would add."
"Laurie is highly competent Engineer. Equally well versed in either Design and Development, or Risk Control methodologies related to Medical Devices; new product development, manufacture, process control, problem identification and resolution, technical file remediation for both Design and Risk controls across very different technologies and device classifications."
Feedback is really valuable to us. If we enabled success in delivering your medical device project, we would love to hear from you.
We grow by recommendation and would be proud to have your testimonial on here.
Let others know about your experience!
"I would wish to have Laurie working alongside me or leading a team I was participating in as the chances of success for that team would be greatly increased. "
"I had the pleasure of working with Laurie, where Laurie was the Project Manager of a major new product development. She demonstrated exceptional enthusiasm, focus, insight, and a keenness to drive forward all aspects of the project, including the clinical use of the technology, ergonomics & usability, regulatory, industrial/mechanical design, manufacturability, as well as the software/electronics development."
"A valued team member and a real team player with natural leadership abilities, applied sensitively, but deliberately when required. Able to garner consensus through effective and efficient collaboration. "
"Laurie was a joy to work with. Her professional dedication and can-do attitude, combined with an ability to focus on small details as well as the bigger picture brought highly valuable skills to the team. I would relish working with Laurie again and would recommend that any potential client gives her serious consideration. "
Are you developing a device and need some compliance help?
Perhaps you would like to implement a QMS or give your current one a refresh?
Got a legacy product technical file needing remediation?
Red Medtech Ltd.
C/O Bevan Buckland Llp, Cardigan House, Castle Court Swansea Enterprise park, SA7 9LA
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Red Medtech Ltd. is a company registered in England & Wales with company number 13474362 - VAT Registration Number 426485577.