YOU SEARCHED BY...

Remove all

SEARCH BY...

Country

Outsourcing Directory


Boulder iQ





Company Headquarters

2840 Wilderness Place
Boulder, CO 80301
United States

Outsourcing Directory

    Related Content

    • Cardiovascular | Neurological
      Imperative Care Closes a Series C Financing of $85 Million for Stroke Treatments

      Imperative Care Closes a Series C Financing of $85 Million for Stroke Treatments

      The funds will support the commercial launch of the company’s portfolio.
      Imperative Care Inc. 12.10.19
    • Diagnostics | Neurological
      RSNA News: MaxQ AI to Offer Accipio Applications on Blackford Platform

      RSNA News: MaxQ AI to Offer Accipio Applications on Blackford Platform

      Represents cost savings and increased quality of care.
      MaxQ AI 12.04.19
    • The Special 510(k) Program—Mike on Medtech

      The Special 510(k) Program—Mike on Medtech

      Mike Drues and Sean Fenske discuss a 510(k) option for modifications to a company's legally marketed medical device.
      Sean Fenske, Editor-in-Chief 11.13.19
    • Cardiovascular | Neurological
      Anaconda Biomed Completes First-in-Human Study of Thrombectomy System

      Anaconda Biomed Completes First-in-Human Study of Thrombectomy System

      Trial Data will support regulatory submission to FDA.
      Business Wire 11.05.19
    • Fiasp Approved for Use with the Omnipod System in the U.S.

      Fiasp Approved for Use with the Omnipod System in the U.S.

      An ultra-fast-acting insulin developed by Novo Nordisk.
      Insulet Corporation 10.29.19
    • Packaging & Sterilization
      Top Surgeons Write Letter to the FDA

      Top Surgeons Write Letter to the FDA

      Stress the importance of Ethylene Oxide for medical device sterilization.
      AdvaMed 10.25.19
    • Cardiovascular
      Corvia Medical

      Corvia Medical's Shunt Device Receives Breakthrough Device Designation

      May reduce symptoms and slow the progression of heart failure.
      PRNewswire 10.09.19
    • Cardiovascular
      Medtronic Stent Graft System Receives FDA Breakthrough Device Designation

      Medtronic Stent Graft System Receives FDA Breakthrough Device Designation

      Developed to treat thoracoabdominal aortic aneurysm.
      Globe Newswire 10.08.19
    • Testing
      Preparing for MDR: Test In-House or Outsource?

      Preparing for MDR: Test In-House or Outsource?

      As the EU MDR deadline draws near, manufacturers are under pressure to bring products into compliance and get submissions in front of regulators ASAP.
      Sandi Schaible, Senior Director, Analytical Chemistry and Regulatory Toxicology, WuXi Medical Device Testing 10.08.19
    • Neurological
      Highmark Interactive Receives FDA Clearance for Gamified Neurological Testing Platform

      Highmark Interactive Receives FDA Clearance for Gamified Neurological Testing Platform

      ‘EQ Brain Performance’ is a tool that addresses cognitive, visual and balance performance.
      Highmark Interactive 10.08.19
    • Surgical
      Top 10 Health Technology Hazards for 2020

      Top 10 Health Technology Hazards for 2020

      The new report identifies safety issues and action steps for 10 dangerous and preventable hazards.
      ECRI Institute 10.07.19
    • New Mobile App Notifies Patients, Caregivers and Nurses of Medical Device Recalls

      New Mobile App Notifies Patients, Caregivers and Nurses of Medical Device Recalls

      SoomSafety aims to close the information gap between the FDA, manufacturers, and medical device users.
      PR Newswire 09.06.19
    • Cardiovascular | Tubing & Extrusion
      Heraeus Medical Components Acquires Via Biomedical

      Heraeus Medical Components Acquires Via Biomedical

      Expands capabilities and development services for catheter technologies.
      Heraeus Medical Components 09.06.19
    • Contract Manufacturing | Machining & Laser Processing
      Biomerics Merges with Northeast Laser & Electropolish

      Biomerics Merges with Northeast Laser & Electropolish

      NLE provides contract manufacturing, laser processing, machining, and metal finishing services to a wide range of medical device manufacturers.
      PR Newswire 08.02.19
    • Digital Health | Software & IT
      Mobile App Notifies Patients, Caregivers, and Nurses of Medical Device Recalls

      Mobile App Notifies Patients, Caregivers, and Nurses of Medical Device Recalls

      SoomSafety is the first mobile app to close the information gap between the U.S. FDA, manufacturers, and medical device users.
      PR Newswire 07.15.19
    • FDA Shares Progress on Efforts to Increase Transparency in Medical Device Reporting

      FDA Shares Progress on Efforts to Increase Transparency in Medical Device Reporting

      Among other changes, the agency formally ended the Alternative Summary Reporting (ASR) Program.
      U.S. Food and Drug Administration 06.24.19