SwipeGuide Co-Founder and CEO, Willemijn Schneyder, shares what’s next in manufacturing technology: Willemijn, thanks so much for the interview. What about your work excites you the most? We’re really excited about what’s happening in the industry today. The manufacturing and heavy machinery industries are moving away from a human-powered, mechanical workforce to become an automated shop floor with tech-savvy workers. Any company’s goal is to be competitive in a connected, data-driven, and ultimately more productive world. But as technology evolves, they’re left with very real problems. Obsolete hardware, difficulty capturing and sharing knowledge, and integration with a new generation of workers all cause major issues for modern businesses.
Read More →Workforce Management Manufacturing: Interview with SchedulePro
Sachin Agrawal is the CEO of SchedulePro, a leading workforce management solution provider for the manufacturing, petroleum and corrections industries, whose customers include Procter & Gamble, a Big 3 auto manufacturer and Shell Oil. As an expert on workforce efficiency and labor cost reduction, Sachin has a track record of significantly increasing productivity and reducing costs for Fortune 500 companies. Prior to SchedulePro, Sachin was a product leader at Microsoft where he developed enterprise-scale products for Windows, MSN and Windows Server. Prior to the American Manufacturing Summit, we spoke with SchedulePro to discuss workforce management in the manufacturing industry. This is an excerpt from the interview with SchedulePro: “Why should manufacturers choose automated employee scheduling over manual scheduling? Increased productivity and the ability to quickly improve their bottom line are two of SchedulePro’s most significant benefits for manufacturers looking to reduce labor costs and improve employee working conditions. An automated solution will also produce staff schedules that are more compliant than manual scheduling solutions, helping manufacturers avoid issues with regulatory and union bodies.”
Read More →Why You Need a New Quality Management System
With technology rapidly changing, a global market, and competition around every corner, quality is one of the most important factors in manufacturing. Quality in products and process will ultimately keep any organization relevant in today’s marketplace. Additionally, having an efficient, paperless, and compliant QMS System can give an organization a competitive advantage.
Read More →The FDA’s New Approach to Digital Health
Recognizing that their traditional approach to moderate and higher-risk, hardware-based medical devices is not well suited for the more rapid and iterative design, development, and validation phases used for software products, the FDA has created a new Digital Health Innovation Action Plan. One important piece of this plan is the “Software Pre-Certification (Pre-Cert) Pilot Program”. This pilot program, which began on September 1, 2017, is a voluntary program that will enable the FDA to develop a tailored approach toward regulating digital health technologies by looking first at the software developer and/or digital health technology developer, rather than the product. The purpose of this is to streamline the regulatory process for companies with a history of developing and testing quality products. Once pre-certified, that developer would be empowered to make software iterations and changes as needed. The nine participants that have been selected for the Software Pre-Cert Pilot Program are Apple, Fitbit, Johnson & Johnson, Pear Therapeutics, Phosphorous, Roche, Samsung, Tidepool, and Verily. According to the FDA, these participants were chosen as they “represent a wide range of companies and technology in the digital health sector, including small startups and large companies, high- and low-risk medical device software products, medical product manufacturers and software developers.”
Read More →Cost-Effective Range of 48-Hour Pre-Qualified Temperature Controlled Shippers
Using just three types of refrigerants and four shippers to create 12 solutions, the Certis® 2-Day Platform maximizes the number of solutions while minimizing the number of components. The new platform is sized to accommodate 7, 13, 27 and 56 liters of product. Each of the new solutions feature a year round pack-out designed for use in both hot and cold seasons. To learn more about qualified temperature controlled shippers, check out this article by Sonoco!
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!
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