My Green Doctor

MAY 29, 2025

Since its launch in 2010, MGD has been helping healthcare clinics, offices, and systems around the world make practical, measurable progress toward environmental sustainability—without compromising patient care, staff efficiency, or clinic finances. 19 countries have national medical associations that provide MGD resources.

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Barton Associates

JUNE 19, 2025

In fact, hospitals, clinics, and other facilities are already reeling from a shortage of providers and it’s hurting patients— according to the United States Department of Health and Human Services (HHS) , tens of millions of Americans live in areas with shortages of primary care, dental, and mental health professionals.

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Annals of Family Medicine

NOVEMBER 20, 2024

2010), as well as more recent scoping review methodology guidelines described by Colquhoun (2014). This scoping review is the first phase of a multimethod study aimed at providing an in-depth understanding of the complex mechanisms influencing equity of access to primary health care for persons living below the poverty threshold.

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StorytellERdoc

JULY 10, 2014

I originally wrote this piece in December, 2010. Lately, though, it seems the system meant to provide this care is being bogged down by questionable decision-making. Instead of providing emergent care, it seems I spend at least half of my emergency room time now playing doctor to chronic illnesses. To pain control issues.

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My Green Doctor

MAY 3, 2025

The breadth of services provided by modern day medicine is profound. A 2010 research study found that treating two patients per bottle instead of one would decrease plastic waste by approximately 12.69 Eye 24 , 361–363 (2010). Reducing waste can save money for practices and operating rooms, and benefit the environment.

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Common Sense Family Doctor

DECEMBER 14, 2024

Surveillance, Epidemiology, and End-Results (SEER) prostate cancer database found that among men with intermediate-risk prostate cancer (based on pathology and a PSA level lower than 20 ng/mL), active surveillance or watchful waiting increased overall from 5% in 2010 to 12.3% and 6.1%, respectively).

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FDA Law Blog

AUGUST 12, 2024

In February 2010, an oral formulation of BRAVECTO, a medication to treat and prevent fleas and tick infestation in dogs, was the subject of an INAD submitted to the Agency. FDA was required to provide fair notice that it would no longer use the INAD date to start the testing phase. When the U.S. While Nissan et al.

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Myriad Genetics

MAY 20, 2025

It’s encouraging to see patients recognize what we, as healthcare providers, already know—that medications can be an effective option for people struggling with depression, anxiety, and other mental health conditions,” said Dr. Brown. He was elected to serve AAPOR as its Vice President, President, and Past President from 2011-2014.

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FDA Law Blog

SEPTEMBER 30, 2022

Dunn suggested that we look to FDA’s previous approval decisions to understand just how much uncertainty can be accepted, sighting in ALS to previous approval decisions that did not provide traditional efficacy evidence. emphasis added).

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My Green Doctor

MAY 3, 2025

The breadth of services provided by modern day medicine is profound. A 2010 research study found that treating two patients per bottle instead of one would decrease plastic waste by approximately 12.69 Eye 24 , 361–363 (2010). Reducing waste can save money for practices and operating rooms, and benefit the environment.

Healthcare 52

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FDA Law Blog

AUGUST 12, 2021

As a result of this decision, Semglee can now be substituted for Lantus prescriptions without the intervention of a health care provider in accordance with state substitution regulations. Thus, though Semglee is not new to the market, it is for the first time substitutable for Lantus without intervention of a health care provider.

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FDA Law Blog

JUNE 21, 2022

Though the Agency’s memorandum provides little interpretive justification for this new approach, it appears to be based entirely on a superficial change in administrative practice. 2010), aff’g 700 F. 2010); Ranbaxy Labs. 35 U.S.C. § 271(a)(2); see also Teva Pharms. Sebelius , 595 F.3d 3d 1303, 1318 (D.C. Sebelius , 384 Fed.

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FDA Law Blog

SEPTEMBER 11, 2023

Over the years, we’ve blogged on similar initiatives related to the 510(k) pathway.

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FDA Law Blog

APRIL 16, 2024

To address concerns that manufacturers were making minor changes to drugs in order for them to be characterized as new covered outpatient drugs with updated (and higher) baseline AMPs, Congress amended the statute in 2010 to add an alternative rebate for line extensions of oral dosage form single source or innovator multiple source drugs (i.e.,

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FDA Law Blog

NOVEMBER 7, 2021

According to the court, HRSA consistently represented before December 2020 that its 1996 and 2010 guidance documents were non-binding and that the agency had limited authority to issue enforceable regulations regarding contract pharmacy arrangements. The Court’s order provides both sides with reasons to claim success.

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FDA Law Blog

AUGUST 18, 2024

The De Novo process provides a regulatory pathway to classify novel devices for which general controls alone or general and special controls provide reasonable assurance of safety and effectiveness for the intended use. This amendment allowed sponsors with low or moderate risk devices to proactively employ the De Novo process.

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FDA Law Blog

FEBRUARY 26, 2024

This of course, make sense—after decades of experience implementing the Hatch-Waxman, Congress and FDA had learned a few new tricks by 2009/2010. Amongst other things, FDA co-opted many of the same definitions for key terms for implementation of the BPCIA. mg) and the concentration (e.g., mg/mL) for liquid parenteral drug products.

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CDOCS

APRIL 14, 2021

<br /> <br /> In 2010, I upgraded to the Bluecam and also added the necessary armamentarium to be able to produce e.max restorations in office.& & & The 4-Y structure provides 1000 mPa in flexural strength, but also allows me to deliver a restoration that I am happy to see on recall.&

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FDA Law Blog

SEPTEMBER 29, 2021

The 340B program, authorized under Section 340B of the Public Health Services Act and administered by HRSA, imposes a ceiling price on pharmaceutical manufacturer sales to “covered entities,” which are certain health clinics that receive federal funding and certain types of safety net hospitals to provide them drugs at lower prices.

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FDA Law Blog

NOVEMBER 1, 2023

Indeed, recent jurisdictional developments suggest that a wide of array of stakeholders could have standing to challenge the Agency’s attempt to restrict access to commonly used LDTs, including individual laboratories, hospitals, physicians and healthcare providers who routinely use these tests, and patients who depend on them.

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FDA Law Blog

APRIL 3, 2023

In 2010, concerned that manufacturers were making minor changes to a drug merely so that it could be characterized as new covered outpatient drug with an updated baseline AMP, Congress added to the statute an alternative rebate for line extensions of oral dosage form innovator (i.e., NDA or BLA) drugs.

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FDA Law Blog

JULY 13, 2022

This period is seemingly arbitrary given that biosimilars have only existed since 2010, and it’s entirely possible that the development of a biosimilar version of a reference product approved 16 years ago could take longer than a product that was approved 8 years ago. On the final condition, it’s not clear what “incentivizes.

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FDA Law Blog

FEBRUARY 27, 2024

For years after the enactment of the Hatch-Waxman Amendments the PTO interpreted the PTE statute to permit multiple PTEs, provided there are separate, but not necessarily different, regulatory review periods. 2010) , however, the U.S. See Lourie, Patent Term Restoration: History, Summary, and Appraisal, 40 Food, Drug, and Cosm.

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GeriPal

DECEMBER 2, 2022

When was that, 2010? Eric: 2010. This whole conference that Ab puts on, and all of the tools and resources that he provides people and families with dementia are about, how do you build on the remaining strengths? It was titled, Healthy Aging Persons and Their Brains: Promoting Resilience Through Creative Engagement.

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Annals of Family Medicine

NOVEMBER 20, 2024

Context: Appropriate use of medication is a key indicator of the quality of care provided in long-term care (LTC). Objective: To determine whether resident-facility language concordance/discordance is associated with the odds of potentially inappropriate prescribing of antipsychotics (PIP-AP) in LTC.

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StorytellERdoc

JULY 17, 2020

Although I could describe to her our efforts, I wanted her to see for herself the incredible attempts of resuscitation being provided. This essay is an updated version first posted in 2010 and it rings just as true today as it did then. She wholeheartedly agreed, embracing my invitation. As always, big thanks for reading.

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Physician's Weekly

JUNE 19, 2025

The number of nurse practitioners specializing in geriatrics has more than tripled since 2010, increasing the availability of care to the current population of seniors, a recent study in JAMA Network Open found. “We step into places where other providers may not, and geriatrics is a prime example of that.”

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Georgetown Pediatrics & Family Medicine

FEBRUARY 7, 2022

In 1891, Williams opened Provident Hospital, the first medical facility to have an interracial staff. Dr. Williams’ skills placed him and Provident Hospital at the fore-front of one of Chicago’s medical milestones. From 1946-1971, her home in Detroit was a safe space, providing support for black LGBT youth in need.

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BMJ

FEBRUARY 8, 2021

The proximity to campus health clinics may also afford college students greater accessibility to healthcare providers for prescription medications such as stimulants which could end up being misused. For healthcare providers, there should be a recognition that holistic care involves more than just prescribing medications. J Addict Dis.

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FDA Law Blog

OCTOBER 24, 2024

By 2010, about 2000 isolated human genes had been patented in the U.S. In 2010, the Association for Molecular Pathology (AMP), among other organizations, brought suit against Myriad Genetics, challenging the validity of the company’s patents on the BRCA 1/2 genes. HPM is currently representing AMP in unrelated litigation.)

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FDA Law Blog

APRIL 17, 2025

million pounds, or 9,600 tons, of unneeded medication since 2010. DEAs Diversion Control website also lists permanent year-round drug disposal locations and provides other disposal information. DEA has collected over 19.2 So, gather the kids and tell the neighbors, Bring out your meds!

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GeriPal

APRIL 13, 2023

Check out some of their recent work, including: Dr. Holt-Lunstad’s and Dr. Perissinotto’s powerful perspective piece in the New England Journal of Medicine which provides a clinical framework for addressing loneliness and social isolation. I think I feel more comfortable as a provider in trying to support people in their isolation.

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GeriPal

MAY 18, 2023

And then in 2010, the AGS took over because it was sort of wafting out there and people were wondering, when are you going to update it? And we were trying to get funding from different places and then AGS kind of stepped in and so they’ve been the stewards of it since 2010. Who’s going to update it? Mike: Thank you.

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FDA Law Blog

OCTOBER 28, 2021

In 2010, the Patient Protection and Affordable Care Act (ACA) established a mandate requiring coverage for women’s preventive services including contraceptives. 300gg-13(a)(4). 300gg-13(a)(4). However, as recently described in a report issued by the National Women’s Law Center, this guidance is often not followed.

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GeriPal

JUNE 5, 2025

Nursing home, length of stay, I think it was like back in 2010, at the end of life. So usually they’ll make recommendations, maybe some medication adjustments or something like that, and then the provider that’s caring for them in house will take over from there. Alex actually was a. I think senior author. Eric 13:49 Right.

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GeriPal

JUNE 22, 2023

And that grew into a group of volunteers coming back and at least providing support groups, giving those men a place where they could talk at least. So in 2010, there were about 150,000 incarcerated people in California. They didn’t have a mentor, a financial provider, all of those things. They suffered from it.

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GeriPal

AUGUST 25, 2022

That trajectory was in increase from 2000 to say, 2010. I do think the growth of for-profit hospice, so around 2000 to 2010, was beneficial in terms of access. I think that there are some really great for-profit hospices out there that are actually able to provide more services and more open access for patients.

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