• May 14, 2024

    Whether it is paints, adhesives, inks or sealants, one must be able to adequately research and critique the latest developments and advances seeking to replace traditional technologies. Whether the goal is to improve the coating’s performance, cost, or environmental benefits, staying ahead of the market and patenting trends and learning about what innovations matter is where Nerac can assist.

  • January 4, 2024

    Bringing disruptive technology into an organization can be long and often frustrating. Many companies do not attempt to do so until the technology has proved itself, or they are forced to keep up with competitors.

  • October 6, 2023

    Since the early 2000s next-generation sequencing (NGS Assays) has become an invaluable tool in both drug discovery research and clinical/diagnostic settings.

  • October 6, 2023

    Pregnancy ultrasounds are well known. Did you know that its first practical use was for detection of objects, propelled by the sinking of the Titanic in 1912?

  • October 5, 2023

    Pediatric medical devices are critical for proper medical care of children. The connection between innovation and realization is a challenging one.

  • October 5, 2023

    1930 methods for scientific research application spearheads AI/ML pattern recognition predictive modeling in in vitro diagnostics 80 years later.

  • July 7, 2023

    This article explores AI and the some of the potential applications, implications and costs for unprepared industry.

  • May 31, 2023

    In the wake of the COVID-19 pandemic, the world continues to recover from disruptions in supply chain. Regardless of industry, companies have had to react in a timely manner, placing an emphasis on safe operations and ramping up supply of essential ingredients and materials to address the crisis, while some successfully pivoted into new product lines.

  • May 31, 2023

    Dramatic changes to the regulatory landscape for in vitro diagnostic (IVD) medical devices are in the making. Some of the most impactful changes include a new classification of IVDs, an expansion of post market surveillance and the increased need for Notified Body review. Most medical device manufacturers are aware that failure to meet In Vitro Diagnostic Regulation (IVDR) 2017/746 deadlines can result in either failure to obtain a CE marking or loss of a currently valid CE mark. The deadlines, however, are not written in stone.

  • May 30, 2023

    Recycling has been popular for over 50 years, but there are still growing pains.