The evolving regulatory landscape and the accelerated pace of medical device innovation are increasing pressure on medical device developers to speed their time to market while providing higher quality products, at less cost. Navigating this shifting terrain and enabling a quick time to market can often be a challenge. In this eBook, we sat down with Cognition Corporation, compliance and medical device solutions specialists, to gather their insights on the commercialization challenges that medical device developers face and the best practices to overcome them. Check out the eBook below: Medical Device Commercialization Best Practices
Read More →The Benefits of Test Engineering Services for the Entire Product Life Cycle
Medical device developers are under increasing pressure to develop new features and better quality products while speeding time to market. One of the ways that developers are achieving this goal is by adopting automation software that will allow them to streamline their product development and test times without sacrificing quality. Averna, a Test Engineering leader, generated the video below to highlight the benefits of automation software and explain how it can help address some of the biggest challenges that medical device developers face. Check out the video below:
Read More →eBook: A Road Map for Addressing Quality and Manufacturing Challenges in Life Sciences
Medical device manufacturers are operating in a constantly evolving environment. Aging populations, evolving healthcare systems and more stringent regulations will have a significant impact on how medical device developers operate and succeed in the years to come. With the American Medical Device Summit quickly approaching, we wanted to take a closer look at how medical device developers will be able to navigate and thrive in this shifting terrain. Pilgrim Quality Solutions, a leading global provider of enterprise quality management software and services, generated the eBook below to help developers address their most pressing challenges and enable a new collaborative model. Check out the eBook!
Read More →Surface Preparation for Medical Device Manufacturers
Surface preparation is a critical manufacturing process that enables sealing, bonding, painting, coating, printing and cleaning. By utilizing appropriate surface preparation processes medical device manufacturers can speed production, ensure product safety, and decrease the likelihood of recalls. Despite the critical nature of this process the majority of manufacturers are still relying upon outdated surface evaluation methods such as dyne and water break. These current methods lack precision, allows for subjective interpretation, and are often destructive. We sat down with BTG Labs to find out more about the challenges of surface preparation and how manufacturers can effectively overcome them. Check out the eBook below! eBook Surface Preparation for Medical Device Manufacturers
Read More →eBook: Medical Device Development Best Practices
With the American Medical Device Summit quickly approaching, we took the time to sit down with one of our industry partners, Stratos Product Development, to gather their thoughts on the biggest medical device development challenges and the best practices to overcome them. Check out the Stratos eBook to explore : Complications arising from a lack of proper documentation, and how to overcome them. Strategies to speed the product development process while effectively managing costs. Tactics to make product launches more predictable. Regulatory considerations that need to be factored into the medical device development process in the U.S. The benefits of outsourcing innovation. eBook, Medical Device Development Best Practices For more insights into medical device development, commercialization and manufacturing, join Stratos at the American Medical Device Summit 2016 taking place in Chicago on October 5th – 6th, 2016.
Read More →Whitepaper: Transitioning to Agile
Safety-critical industries face many challenges including stringent regulations and requirements, and increased pressure to speed time to market while improving product quality. As a result, it is often difficult for organizations to move away from traditional development processes and integrate agile methodologies. Seapine Software has generated the whitepaper below to help medical device manufacturers overcome these barriers and successfully transition to agile in a safety-critical environment. To hear more from Seapine Software, join the discussion at the American Medical Device Summit taking place this October!
Read More →Operational Efficiency Whitepaper: Beyond Compliance
dMedical device manufacturers are facing increasing challenges in the development, production and commercialization of their devices. To offset rising costs, evolving regulations and increased pressure to speed time to market, manufacturers are streamlining their processes and implementing strategies that drive operational efficiency. Dassault Systemes has generated an informative white paper to help medical device developers drive innovation and improve operational efficiency by creating processes that incorporate quality, engineering, and regulations. Download the “Beyond Compliance” whitepaper to learn how to Connect the Dots Between Quality, Engineering, and Regulatory to Increase Innovation and Improve Operational Efficiency. To hear more from Dessault Systemes, Join the discussion at the American Medical Device Summit 2016 taking place in Chicago on Oct 5th – 6th, 2016.
Read More →Infographic: 5 Mistakes That Can Derail Your Medical Device Development
Medical device developers have a series of hurdles they need to navigate in order to successfully bring their device to market. In today’s infographic, we explore the top five mistakes that can derail the medical device development process and consequently speed to commercialization. Check out the Infographic: 5 Mistakes That Can Derail Your Medical Device Development For more insights into medical device development, commercialization and manufacturing, join Stratos at the American Medical Device Summit 2016 taking place in Chicago on October 5th – 6th, 2016.
Read More →Medical Device Infographic: The Recall Impact
In today’s post we draw on the expertise and insights of EngiSystems to examine the growing impact of recalls in the medical device industry. The infographic below illustrates the increase in medical device recalls over the past decade and outlines some of the major challenges that have lead to this increase. Infographic: The Recall Impact For more medical device insight. join EngiSystems at the American Medical Device Summit 2016 taking place in Chicago on October 5th – 6th, 2016.
Read More →eBook: Traceability Optimization for Medical Device Developers
Regulatory bodies such as the FDA require medical device manufacturers to document and track huge amounts of information to ensure device safety and demonstrate that safety in the event of an audit. Given the volume and complexity of information to be tracked, many medical device developers struggle with traceability. We sat down with Seapine Software to better understand the challenges medical device developers face, and how they can be overcome. Check out the Traceability Optimization eBook below! eBook, Traceability Optimization for Medical Device Developers
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