Medical Device Product Lifecycle Management and Manufacturing
Providing Medical Device Product Lifecycle Management Solutions
Developing, manufacturing, and launching a new medical device seems like a daunting process, and nurturing the product’s success after it’s on the market seems even more complex. With Remington guiding you through your medical device’s product lifecycle management (PLM), you get a seamless path to a successful product for years to come.
Medical device PLM is about more than just getting your product on the market. Once the product is available, there’s still consistent work to be done. Remington Medical is with you every step of the way. From design strategy to product launch and beyond, once you trust us as a committed manufacturer, you get a lifelong partnership.
We develop a medical device commercial strategy for every product we take on. We consider device classification, product life cycle, regulatory requirements, testing, and the launch of the end product.
The one question on every contract manufacturer’s mind is, “How long will it take for my device to launch?”
The simple answer: every product is different. The design, materials, and processes are all factors that play a part in a timely launch date. No matter how long the product launch takes, we keep you informed and involved every step of the way.
When you bring medical devices to an evolving market, you have to consider the time it takes and how to meet the demands of global supply chains. Remington has experience in overcoming these challenges while delivering high quality manufacturing. Our team will be there in the future to keep up our standards and manage your product’s supply chain, from manufacturing to distribution.
In the medical device manufacturing industry, the manufacturer of record is the entity that FDA considers the product manufacturer. Since different companies and suppliers are involved in designing and manufacturing medical devices and supplies, it’s crucial to distinguish who’s liable for the device early on. Remington is an experienced medical device manufacturer of record. If an audit occurs after your medical device is on the market, we work with you and the FDA to clear up any confusion.
Nurturing your product’s success with our PLM solutions is the final step of our proven process for contract manufacturing. Before developing a seamless path to a successful medical device after its launch, we establish a relationship with you, conduct extensive research based on your product needs, and create a custom manufacturing process that solves complex problems before they arise.
Our dedicated approach to meeting your needs is what makes us stand out among other medical device manufacturing companies.
When you choose Remington, you get:
Our product packaging service includes testing the material for quality assurance before it leaves our facility. We’ll even help you create a design and suggest the best material option, depending on your product. We believe that no device is created equal, so we customize your packaging to meet the needs of your device materials.
Proper sterilization is mandatory for device manufacturing. The Food and Drug Administration (FDA) monitors the sterilization process to ensure all manufacturing companies are compliant. Remington Medical takes away the stress of compliance by communicating directly with the sterilization vendor of your choosing. We get your product to the vendor and ensure they perform a sterilization run that meets all applicable international standards.
We developed a customized testing methodology dedicated to the quality assurance of your packaging. Our methods ensure that the material shelf life preserves your product’s quality and integrity. The results lie within the details. That’s why our team never misses a single factor that could result in a poor-quality product.
Remington offers everything you need to develop and manufacture your medical device, including your medical device PLM after launch.
Remington Medical specializes in taking clients through every step of the manufacturing process from product development to the manufacturing phase. By committing ourselves to our customers, we are dedicated to your device’s success from start to finish. We pride ourselves on our superior product development and innovative manufacturing, making us your single source for medical device manufacturing.
Our project team turns complex production runs into manageable projects. Due diligence is encompassed in our manufacturing approach, so you can expect caution and care to lead the way to a successful product launch.
Designing and manufacturing medical devices require extreme attention to detail. Our experienced team encounters each step of the process with a meticulous set of eyes. We don’t compromise quality for large-scale projects. You can expect us to get it right the first time and consistently deliver quality results afterward.
Remington implements the proper steps to continue the process seamlessly. It takes an entire team to come together to ensure each step is represented and delivered to the end. That’s we have a dedicated team that specializes in:
It’s our goal to deliver superior products to your customers every time.
At Remington Medical, we’re passionate about holding ourselves to a higher standard, and we care about your medical device PLM just as much as you. From product conception to design, delivery, and post launch, Remington is here to support your success, helping you create the best product possible. We don’t just focus on today’s product—we think about the future of your business and the future of medical technology.
The one question on every contract manufacturer’s mind is, “How long will it take for my device to launch?” The simple answer: every product is different. The design, materials, and processes are all factors that play a part in a timely launch date. No matter how long the product launch takes, we keep you informed every step of the way.
We develop a medical device commercial strategy for every product we take on. We consider device classification, product life cycle, regulatory requirements, and testing.
We never stop improving. That’s one of the reasons why we established our own in-house specialty tooling shop. As a part of our product lifecycle management manufacturing process, we’ve trained our team in different tooling techniques, such as:
Remington is compliant with FDA regulatory requirements. Our notified body, the British Standards Institution, has certified us in ISO 13485, an international standard for quality management. We also work closely with many organizations nationwide, including:
At Remington Medical, we strive to bring you the best FDA registered medical devices on the market. We check each one of our products in-house to ensure you receive a high-quality device every time. Contact us today to learn more about our approach to medical device manufacturing.
Contract manufacturing and high-quality medical devices to meet your needs. Contact Remington to see how we can bring value to your organization!