Eurofins Lancaster Laboratories PSS Insourcing Solutions is a program that places a team of experts in the client’s laboratories with access to their quality systems in order to execute a project in the client’s scope of work. By adopting this insourcing approach, organizations are able to benefit from the expertise of an experienced laboratory testing provider, while reducing costs as they continue to keep projects, methods and analytical techniques in-house. With more than a 55-year track record of scientific and laboratory operations expertise, PSS ensures that each team of experts are top quality and selectively chosen for the appropriate project. This in-house approach is preferred by pharmaceutical and biopharmaceutical companies as opposed to hiring temporary staff. Temporary staff solutions result in valuable resources being used for recruitment, training, and managerial purposes, which could be redistributed to another area. Temporary staff also often result in conflicts with long-term needs, European regulations, and strict IRS guidelines. Benefits of insourcing include lower headcount, avoiding high turnover, condensing product development cycles, flexibility and more. PSS’s Insourcing Solutions has grown exponentially, currently, employing more than 1,500 employees, as well as serving clients in 15 countries at more than 70 different sites worldwide. You can find more information on the PSS’s Insourcing solutions in their ebook here. For more information on Eurofins, visit their website here.
Read More →Temptime Ebook: Key Issues in t he Storage & Transportation of Temperature-Sensitive Medical Product s
Temptime innovates cost effective monitoring solutions for environmentally sensitive products to ensure supply chain integrity, protect patients and benefit communities globally. The emergence of the storage and transportation of temperature-sensitive medical products has given Temptime the expertise and knowledge to resolve prevalent issues in this field. Temptime has narrowed down the key issues to the following: – Evolving Regulatory Oversight – Customer Complaints & Patient Safety – Impact on Financial Performance Temptime has identified that organizations have a challenge balancing the requirements of regulators and the needs of patients when adhering the temperature monitoring regulations. Another challenge is reducing costs and positively impacting the financial performance of a company. Temptime has unique solutions that can significantly reduce product returns and gain a competitive advantage in the market by enhancing the customer experience. For more information on key issues and solutions in the storage and transportation of temperature-sensitive medical products and solutions, read Temptime’s ebook here. To visit their website, click here.
Read More →Averna’s Q&A Ebook: How the Internet of Things is Transforming the Medical Device Industry
The ‘Internet of Things’ is transforming the medical world, allowing more patients to be looked after using real time data. Combining Wi-Fi and Bluetooth capabilities with current technology is allowing for a faster, more resourceful and satisfying experience for both patients and employees. With the Internet of Things(IoT) reinventing the technological landscape so rapidly, companies are struggling to keep up with the latest innovations. Companies must now test the wireless capabilities of all their medical devices to ensure their products feature seamless connectivity. With more tests being conducted and the rise of IoT, competing companies have introduced robots to automate processes in order to reduce costs. Robotic-driven production has become more economical, as robots can perform routine tasks without fatigue at a faster pace. So, how can OEMs in the medical world stay ahead of their competition with all this technological development? One way is to work with a company that excels at Design for Test (DFT) and design for manufacturing (DFM). Companies can also capture and analyze up-to-date test data. For more ways to stay ahead of the competition despite the constant changes in technology and for a deeper understanding of IoT and its impact on the medical device industry, read Averna’s Q&A Ebook here. Averna is a worldwide Test & Quality leader. Their talented team includes hundreds of engineers, system architects, developers, project managers and other professionals, as well as a network of partners such as National Instruments, Keysight Technologies …
Read More →Flexible Circuit’s Ebook: Information and Applications for the Medical Device Market
Flexible Circuit’s ebook explores and identifies solutions to the following industry challenges: How have intelligent devices(and the ability to share realtime data) driven significant growth of electronics within the medical device market? What is driving the significant use and growth of Flexible Circuits (FPCs) in the medical device market? What are the key considerations in choosing an FPC manufacturer? How can organizations attain cost savings when using flexible printed circuits? To view their full e-book, click here.
Read More →Let Solid Designs help you develop new products & create manufacturing solutions!
Solid Design Solutions provides assistance with the development of new products and creates manufacturing solutions for a number of industries, which include: consumer, medical, specialty machines and industrial. Some of their areas of expertise include: Control engineering Project management Manufacturing engineering Industrial design Software Engineering Mechanical Engineering Electrical Engineering Product Development Research Drafting More details on the type of services they offer can be found here: https://generisgp.com/wp-content/uploads/2017/09/Inforgraphic-final.pdf Solid Design Solutions Website: http://bit.ly/2eMae5b
Read More →Verification Stations for 10 Different Advanced Medical Devices
“The Challenge: Are there any devices more life-critical than those used by our doctors and nurses? You want to be absolutely sure that each one will work exactly as designed, 100% of the time. That’s why there is so much oversight on the industry. Every player needs to get it right.” Averna and Spacelabs Healthcare has collaborated to create a verification station that can test 10 different medical devices. Their case study explores the results and benefits of this project. For more information, click here.
Read More →Are you struggling with finding a fully validated Requirements Management Tool?
“Validation is required, as regulated by FDA, to ensure that a company’s product development software/system will meet its intended purpose. The software/system must show that it will function in a reliable, consistent manner and is in compliance with regulatory and business requirements. Additionally, once the software/system has been accepted and released for use, there is a need to maintain compliance and fitness throughout its operational life. Unfortunately, information on how to develop a validation plan and the activities expected as part of a validation effort are limited and subject to misinterpretation.” Are you struggling with finding a fully validated Requirements Management Tool? If so, check out the full white paper by Cognition!
Read More →Major Test Challenges For RF Products
This PDF by Averna will delve into: Higher and higher frequencies More RF standards, fewer test resources Increased Takt time and slower throughput Capturing large instantaneous bandwidths Streaming large amounts of RF data Click on the link below to check out the full PDF about the major test challenges for RF products! http://bit.ly/2eLmdmy
Read More →Q&A eBook with QT9 Software: Benefits of Automating Your Quality Management System with Software
Industry regulations can make life for medical device manufacturers very challenging. Regulations are there for a reason and are required to grow and improve your business. This is different than in most manufacturing sectors. Demonstrating compliance to these various regulations requires meticulous record management. As an example; the ability to easily manage and maintain your records for Product Design, can provide an organization with a competitive edge for getting new products, or enhancing existing products for their market. QT9 Software will be speaking at our American Medical Device Summit taking place October 4-5th, 2017 in Chicago, IL. The presentation topic will be on the “Benefits of Automating Your Quality Management System with Software.” We asked Brant a few questions about quality management, issues medical device manufacturers are facing today, and how to save time and money in the industry. Please, take a look at our Q&A eBook with Brant Engelhart from QT9 Software below!
Read More →Industry Insights: Interview with Dr. Steve Levine, Dassault Systèmes
At Generis’ American Medical Device Summit 2016, we sat down with Dr. Steve Levine, Senior Director of Product Strategy and Executive Director of the Living Heart Project at Dassault Systèmes and discussed scientific innovation initiatives such as the Living Heart Project, realistic simulation, and technology’s role in the industry. Check out the full video below!
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