Healthcare

WHITE PAPERS AND CASE STUDIES

• ABB Technology Helps Equip New Zealand With A More Resilient Water And Wastewater Infrastructure

  All around the world, issues such as surging energy costs, scarce resources, population growth, and climate change are making securing water in a sustainable way increasingly difficult. Here’s how New Zealand is future-proofing its water system.

• Diving Into Smart Water Management

  Learn about a water management project that established a culture of innovation and smart water management for the coastal city of Porto. 

• Mobile App And Wearable Integration Collects Longitudinal Data

  Get an overview of SISCAPA's utilization of eTechnologies, specifically ePRO, and how their partnership with CDS accurately demonstrates the improvement of data collection and analysis in the biotechnology industry.

• Water For Life: ABB’s Measurement Technology Trailblazes Water Solution

  Pioneering sustainable water supply with the world’s first dual mode desalination plant.

• How To Run Successful Clinical Trials In Japan

  Read about why there is no longer any excuse not to include Japan as an integral part of any global clinical-development program for either pharmaceuticals or medical devices. 

• Measuring Laser Output In Medical Equipment Manufacturing For FDA Approval

  With expertise in power and energy measurement for lasers, see why Gentec-EO is the go-to choice for medical manufacturers in need of accurate and reliable laser beam measurement solutions.

• How To Save 9k Hours And Cut Deviations By 27%

  This pharma company transitioned off paper, slashing their deviation count and saving thousands in onsite hours. Learn how they were able to streamline business operations and free up resources.

• Making Intelligent Connections Possible: Connected Devices – Better Devices

  The demand for connected devices in clinical trials has grown significantly, driven by a need for better, more varied data, and renewed bids to improve patient experience and reduce the burden for trial sites.

• Navigating The Privacy Tightrope For CTIS

  Examine the challenges, potential risks, recommended best practices, and future trends related to anonymizing personal data for Clinical Trials Information System submissions.

• The Regulatory Evolution And Data Revolution In Medical Device Development

  The Life Sciences and Healthcare industries are among the most heavily regulated industries in the world. This paper looks at the current, dynamic regulatory landscape within the medical devices sector and some of the current and future changes medical device organizations will need to adhere to. The in-vitro diagnostics (IVD) sector is also going through regulatory change - a topic that is out of scope for this paper.

• Choosing An EDC With A Robust API For DTx Clinical Trials

  This white paper explores the importance of choosing an EDC with an API before starting a clinical trial.

• Could RFID-Based Unit-Level Traceability Be Key To Operational Excellence?

  Radiofrequency identification (RFID)-based unit-level tracking solutions for prefilled syringes are poised to help pharma manufacturers address key risks and costly bottlenecks related to the fill-finish process.