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DIGITAL PATHOLOGY: A Primer for Microscope Camera Selection

Most pathologists today use digital systems within their practices and research projects to communicate, store data, and analyze images. Whether it’s within clinical, forensic, surgical, or other branches of pathology, communication and consultation among specialists is greatly improved by the use of digital systems and enables faster diagnosis for patients.

Posted in: White Papers, Imaging, Medical, Optics, Photonics

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Avoid the Dark Side of Quality Failure

Revealed in this eBook is a new hope that unites product lifecycle management (PLM), quality management solutions (QMS) and application lifecycle management (ALM) to enable product companies to overcome the phantom menace of global competitors and stricter compliance mandates to save the universe with great products. Your company’s team of quality experts, operation managers and engineers will learn how to embrace the power of an all-in-one product development solution.

Posted in: White Papers, White Papers, Bio-Medical, Medical

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IoT Device Battery Analysis

Explore how engineers address the consumer, industrial and medical demand for ever-longer battery life from IoT devices. Learn the tools used to provide insight into an IoT device’s complex battery consumption waveforms and how designers and manufacturers can create new ways to extend the battery life. Download Application Note.

Posted in: White Papers, White Papers, Energy Efficiency, Electronics & Computers, Bio-Medical, Medical

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Planning for Implementation of the European Union Medical Devices Regulations – Are You Prepared?

The Medical Device and In Vitro Medical Device Regulations represent the most significant change to the European legislation for medical devices for nearly 20 years. Understanding the requirements is key to your ability to develop an implementation plan to ensure continuing regulatory compliance and provide the EU market with safe medical devices.A new white paper, “Planning for Implementation of the European Union Medical Devices Regulations: Are You Prepared?” focuses on the practical aspects of implementation. It discusses decisions that need to be made and includes questions to ask about your organization’s preparedness to comply with the new requirements.Download this new white paper to learn how to address: Activities and requirements for manufacturers, authorized representatives, importers, and distributors Existing products and their technical documentation, including clinical evidence Products in the development pipeline Responsibilities of the person handling regulatory compliance, ISO 13485:2016 certification, and lifecycle management Content and maintenance of technical documentation Unique device identification, implant cards, and labelling changes PMS plans, periodic safety update reports (PSURs) or post-market surveillance reports, and post-market clinical follow-up (PMCF)

Posted in: White Papers, Manufacturing & Prototyping, Bio-Medical, FDA Compliance/Regulatory Affairs, Medical

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Ensuring the Reliability of Disposable Syringes with Light-Cure Adhesives

Perhaps one of the most challenging aspects of disposable medical syringe production involves permanently and safely attaching the stainless steel cannula to the plastic hub. This joint is critical to the safety of syringes found on hypodermic and biopsy needles, syringes, winged infusion sets, blood lancets, and a variety of other devices. In all these applications, poor hub-to-cannula assembly could result in leakage of bodily fluids and medication or catastrophic device failure, situations that could be dangerous to the patient and the medical professional. Mechanical failure of a syringe can cause painful insertion or extraction, seal failure during use, cancellation of a procedure, or other unsafe complications.

Posted in: White Papers, White Papers, Bio-Medical, Medical

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The Simple Guide to a Life Science Recall

Recalls erode consumer trust, brand integrity, company image and longevity. Since there is a lengthy process that follows the event of a recall, here is how a GMP Compliance Management System can help to make the process as efficient, painless and quick as possible.Download this paper to learn about: Complaint Handling Product Returns Document Control Recall Evaluation Corrective Action Centralized Reporting

Posted in: White Papers, White Papers, Bio-Medical, Medical

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Life Sciences Guidebook: Best Practices for FDA Compliance Solutions

In a market where high-demand causes organizations to seek software systems that will fit into their complex business infrastructure, the pressure to find the right system often causes angst to many. Learn some of the key elements to spotting a good FDA Compliance solution, techniques for achieving GMP Compliance, and how to ensure that Quality and Compliance are met in the Life Science industry.

Posted in: White Papers, White Papers, FDA Compliance/Regulatory Affairs, Software

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