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Related Concept Videos

iChip01:24

iChip

The cultivation of environmental microorganisms has long been hindered by the inability to replicate complex native conditions in vitro. The isolation chip (iChip) addresses this limitation by facilitating the growth of previously uncultivable microorganisms through in situ incubation. Designed for high-throughput microbial cultivation, the iChip comprises hundreds of microchambers, each capable of housing a single microbial cell. These microchambers are loaded with a mixture of molten agar and...
Non-ohmic Devices00:51

Non-ohmic Devices

In most substances, the current flow is proportional to the voltage applied to it. A simple relationship between the values of current, voltage, and resistance is known as Ohm's law. Nonohmic devices do not exhibit a linear relationship between voltage and current. One such device is the semiconducting circuit element known as a diode. A diode is a circuit device that allows current flow in only one direction.
Consider a simple circuit consisting of a battery, a diode, and a resistor. A diode...

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Updated: May 16, 2026

Rapid and Low-cost Prototyping of Medical Devices Using 3D Printed Molds for Liquid Injection Molding
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Creating a space for innovative device development.

Michelle McMurry-Heath1, Margaret A Hamburg

  • 1Office of the Center Director, Center for Devices and Radiological Health, U.S. Food and Drug Administration (FDA), Silver Spring, MD 20993, USA. michelle.mcmurryheath@fda.hhs.gov

Science Translational Medicine
|December 5, 2012
PubMed
Summary
This summary is machine-generated.

The U.S. Food and Drug Administration (FDA) is partnering with the Medical Device Innovation Consortium to improve regulatory science for medical technologies.

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Area of Science:

  • Regulatory science
  • Medical technology innovation

Background:

  • The medical device landscape is rapidly evolving.
  • Advancing regulatory science is crucial for ensuring patient safety and access to innovative medical technologies.

Purpose of the Study:

  • To announce a strategic partnership between the FDA and the Medical Device Innovation Consortium.
  • To foster collaboration aimed at enhancing regulatory science within the medical technology sector.

Main Methods:

  • Establishment of a new nonprofit organization: the Medical Device Innovation Consortium.
  • Collaborative efforts between the FDA and the consortium to address regulatory challenges.

Main Results:

  • A new public-private partnership is formed.
  • Initiatives to accelerate the development and review of novel medical devices are expected.

Conclusions:

  • This partnership signifies a commitment to modernizing medical device regulation.
  • The collaboration is poised to drive innovation and improve regulatory pathways for medical technologies.