Published on : 2017-04-16 08:18:26

This is a topic worthy of significant attention and consideration. Second, we want to more clearly define the guiding principles that the scientific community should consider in designing product features that achieve these possible solutions. Our goals at this scientific workshop encompass three key areas. Finally, we’ll better define the types of data needed in order to evaluate how these solutions are working. In the setting of the President’s declaration of a national public health emergency related to the crisis, I’m reaffirming the FDA’s commitment to work across the full range of its authorities to address this epidemic. That is why today we announced a two-day public workshop, which will take place on Dec. There are a number of new steps the FDA is considering. The Opioid Policy Steering Committee that we established in May is considering, among other things, what steps the agency can or should take with respect to packaging (e. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.

11-12, 2017, to advance this issue by working with a broad set of federal, state, and other stakeholders who are also addressing the challenges of balancing pain management with the critical need to address the opioid epidemic. To achieve these goals, one area we’ve committed to exploring further is how opioid drug products are packaged, stored and ultimately – when no longer needed – discarded. At the FDA, we’re especially focused on helping more patients struggling with current addiction receive appropriate care with proven treatments and reducing new cases of addiction. The FDA has already been working on several efforts to explore solutions in this area. When prescriptions are initially written, they should be for durations of use that comport with the clinical circumstance. We also have created an internal task force that’s conducting additional research to inform our policies and decision-making in these areas. First, we need to define the specific problems that these types of packaging and disposal solutions can help address. Other packaging innovations could make it easier to track the number of doses that have been taken. The FDA is committed to exploring our existing authorities to find new and impactful ways of regulating these product features to improve patient safety.

For example, it’s possible that a defined, short-term supply of medication could be packaged in a manner that limits the number of pills dispensed. There are also technologies that could allow health care providers, pharmacists or family members to monitor patient use of prescription opioids. , on new strategies for addressing the crisis of opioid addiction through innovation in packaging, storage and disposal Statement One of my highest priorities as the Commissioner of the cam girl home looking model video web work.
. We look forward to the two-day meeting and the opportunity to discuss the potential for new, innovative tools and strategies the FDA can take to address the public health crisis of opioid addiction. This might be achieved, for example, through a blister pack that has a defined duration of use that might be for only a limited number of doses. Food and Drug Administration is to take whatever steps we can to reduce the scope and human tragedy created by the epidemic of addiction to opioids. Lowering the rate of new addiction means also reducing overall exposure to opioids to prevent more people from becoming addicted to these drugs in the first place mandating additional. , unit of use) to facilitate appropriate opioid analgesic prescribing practice. .

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SOLAS amendments on additional means of escape from machinery spaces agreed The Sub-Committee agreed draft amendments to SOLAS mandating additional means of escape from machinery spaces, for submission to MSC 92, for approval with a view to subsequent adoption.

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