Medical Murray is a medical device development company that specializes in testing of both components and devices to support regulatory filings, validations, and market comparison studies. Testing may be performed either in conjunction with the regulatory process or as a standalone project. Examples of our internal services include:
Complete testing expertise is offered including mechanical and functional testing.
For testing activities, selecting qualified testing laboratories is essential. Regulatory bodies expect testing to be performed by qualified laboratories. Asking regulatory bodies such as FDA to accept test data from an unaccredited testing facility would be a challenging endeavor and ultimately end in failure.
The key for medical device manufacturers is to have a strong understanding of the limitations their testing suppliers might face. Medical device manufacturing companies have to look for deficiencies in their supply chain and take steps to correct or mitigate those problems. Recognizing these deficiencies is half of the battle when it comes to organizations pursuing the appropriate steps to preclude making the same errors. Some of the most common deficiencies includes:
Complete testing expertise is offered including mechanical and functional testing.Our onsite testing laboratories offer an ability to provide customized testing to meet your specific needs.
Choose the correct medical device company with strong testing servies. Choose Medical Murray.
Our team would like to help you create and implement your next medical device development project. Please contact us or visit our website for more information.
Call us at: 847.620.7990
Email us at: email@example.com
Medical Murray provides and develops extensive testing services. Let our engineers work with you to develop a custom test procedure specific to your device or component. Our onsite labs feature an extensive inventory of testing equipment to provide accurate data and analysis.
We specialize in testing to support regulatory filings, validations and market comparison studies either in conjunction with the development process or as a standalone project.
Examples of our internal services include:
At Medical Murray, we utilize standard ISO, ASTM or FDA methods. All testing is performed according to pre-approved protocols, and conforms with required ISO and FDA standards.
Our team would like to help you create and implement your next medical device project. Please contact us or visit our website for more
A good medical device manufacturer needs to provide fully comprehensive development services for the creation of your medical device with extensive knowledge of catheter design, implant design and catheter component assembly. It is essential that the medical device manufacturer offers original designs as well as custom processes. The team should work with you to define every aspect of your concept.
Vertical integration should also be a core strength of the medical device manufacturer that you choose to work with, including:
If you have any questions about medical device manufacturing, contact Medical Murray to see how we differ from other companies!
We offer comprehensive development services for the creation of your device with extensive knowledge of catheter and implant design.
At Medical Murray, our team of engineers deliver creative design services based on a combination of a quality education, varied medical device development expertise, and state-of-the-art software tools. Our extensive knowledge of catheter design, implant design, and catheter components assembly enables us to provide a complete medical device. Our team will work with you to define every aspect of your concept including:
Medical Murray, a medical device development company, provides pilot production of devices for use in regulatory testing, device demos, animal studies, and clinical trials. We utilize Class 7 certified clean rooms for pilot production in all of our locations (Illinois, North Carolina and California).
At Medical Murray, your medical device pilot production is supported with dedicated clean rooms and production resources.
Builds are completed using released documentation and materials, utilizing an ISO 13485 quality system that ensures safety yet allows for flexibility. The pilot manufacturing stage brings together design engineering, process development and quality systems to refine production processes and inspection requirements for volume manufacturing.
Our pilot production services include:
Our assembly team offers extensive expertise in intricate devices often requiring assembly and inspection under a microscope. Assembly expertise includes custom tipping, handle assembly, multi-layer laminations, insert molding, and much more.
The Medical Murray quality team is dedicated to ensuring that the devices we manufacture are of the highest quality, certified to ISO 13485, and are cGMP compliant.
Our quality engineers are involved in the development stages of all projects to identify and develop quality requirements, test methods, and inspection requirements that are used to validate new products.
Whether you’re looking for a finished device, component part, sterilization, bulk or packaged product, we can ramp up your product for commercial release.
Looking for medical device development companies to assist you with manufacturing your medical devices? Please contact us or visit our website for more
Medical Murray is FDA registered
and can handle your full sterilization,
packaging and distribution needs.
Our complete range of manufacturing capabilities, and the ability to create custom equipment, allows us to produce complex, intricate devices to your specification. We are dedicated to the production of class II and class III medical devices in ISO class 7 clean rooms.
Our assembly of complex disposable and implant devices adheres to comprehensive traceability and strictly enforced written procedures at each step of the manufacturing process. We are fully equipped with machinery including injection molding machines, braiders and custom forming equipment.
Production services include:
Our team would like to help you create and implement your next medical device project. Please contact us or visit our website for more information.
Our prototyping labs, located at our medical device development facilities in Illinois, North Carolina and California, equip the engineering team with capabilities and resources to meet client requirements quickly - resulting in rapid assessment of form, fit and function. Our laboratory is equipped with a wide range of equipment, including:
Our development process and its documentation comply with FDA 21 CFR Part 820 as implemented through our ISO 13485 certified Quality System.
The pilot production stage brings together design engineering, process development and quality systems to refine production processes and inspection requirements for volume manufacture. Pilot production devices are built in one of our dedicated clean rooms with production resources. Using released documentation and materials, these builds support validation testing, animal trials, clinical trials, and market release.
Our team would like to help you create and develop your next medical device project. Please contact us or visit our website for more