Micro Machines to be used in hospitals, universities, etc.
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Micro Machines will soon be used to deliver medications to patients, even though they’re currently not approved for that purpose.
The Food and Drug Administration is working on a rule to require such micro-machines, known as injectors, to undergo a rigorous safety review, which will make it easier for them to be placed in hospitals and other health facilities.
The FDA is expected to make a final rule in the coming weeks, but experts said that there will likely be plenty of time for the process to unfold before the end of the year.
There are also signs that the technology is finally starting to catch on in other industries.
Last year, Apple, Amazon and other big tech companies began testing and certifying the safety of the injectors in the food supply.
Micro Machines, also known as “batteries,” are being used in home appliances and food-processing equipment, and in some consumer electronics.
In the food industry, a micro-chip that can be programmed to perform a specific task, such as adding sugar to a dish or removing food debris, is an important feature for the safety and efficiency of food packaging.
The injectors are used for these applications, but not for drugs or vaccines, because they aren’t approved by the FDA to be injected directly into the bloodstream.
They are only approved for use in the manufacturing of medical devices and for use as dispensing devices for injections.
The agency said that its proposal is designed to address the need for injection safety, and will not affect any existing micro-machine applications.
But for the micro-device companies, the agency’s rulemaking is a huge step toward getting the injection process down to a science.
“Micro machines are the future,” said Andrew T. Cusick, chief executive of Biosys Inc., a San Francisco company that makes injectors.
“Micro machines were once just a toy, a niche product, a novelty,” he said.
“Now they are part of the fabric of life.”
The rulemaking process began when the FDA issued an interim guidance to the medical device and food industries in December.
It was issued without public comment, but in the interim, a number of industry groups sent letters to the agency asking for the rule to be reconsidered.
The letter said that micro-mechanics are “a promising tool for the development of the next generation of micro-processors,” and that the rulemaking could lead to the development and use of the technology for the “precision, rapid, and affordable delivery of therapeutics, vaccines, and medical devices.”
The FDA has not yet made a final determination about the rule.
If it does, it will likely come in the form of a guidance that sets guidelines for the regulation of injection safety and the industry will likely have another round of negotiations with the agency.
“The rule could have a profound impact on the pharmaceutical industry, and the health care industry as a whole,” said Peter W. Meehl, a professor at the University of California, San Francisco School of Medicine who specializes in the intersection of medicine and technology.
Micro-mechs are a new class of microdevices.
They were developed by researchers at Stanford University, which is working with a variety of companies to develop medical devices.
The industry has had some setbacks in the past few years, however.
Micro-mecha makers have struggled to convince regulators that their technology meets regulatory requirements, and a 2014 FDA study showed that only 1 percent of the devices manufactured by micro-engineering companies met the agency-approved safety standards.
In October, a coalition of drug makers called the Pharmaceutical Research and Manufacturers of America said that some injectors used in the medical industry “are not currently being tested and certified by the U.S. Food and Drugs Administration.”
The group, which includes such big pharmaceutical companies as Abbott Laboratories and Novartis, said that the injection devices were not properly labeled, and that they “should be treated as dangerous drugs.”
Micro Machines will soon be used to deliver medications to patients, even though they’re currently not approved for that purpose.The…
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