Search for: "Medical Authorization Review"
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13 Sep 2011, 7:09 am
Patrick Hosp. that a Medical Review Panel's finding is not subject to mandatory admissibility when the Medical Review Panel exceeded its statutory authority by making its determination based on of a finding of credibility. [read post]
2 Jun 2023, 11:01 am
US border authorities released a statement Thursday disclosing that the eight-year-old girl who died while in their custody last month was denied attention or review from medical staff. [read post]
24 Aug 2015, 6:30 am
Author Michael Stack, Principal, COMPClub, Amaxx LLC. [read post]
11 Sep 2013, 6:30 am
Author Rebecca Shafer, JD, President of Amaxx Risk Solutions, Inc. is a national expert in the field of workers compensation. [read post]
14 Feb 2012, 4:09 am
The Medical Review Panel also is allowed to consult with other medical authorities when reviewing the matter. [read post]
12 Jun 2013, 5:16 am
One of the big controversies that has surrounded utilization review (UR), and now independent medical review (IMR) is whether the physicians conducting these reviews were engaged in the "practice of medicine" and thus subject to review, and possible discipline, from the medical board in the state where the case originates.At least in California, the Medical Board has recently opined that UR and by extension IMR is the practice of… [read post]
20 Jun 2022, 11:34 am
The post Amendment Regarding Venue Authority for Civil Lawsuits Under Review appeared first on Wieand Law Firm. [read post]
12 Apr 2023, 9:01 am
What Is an Independent Medical Review? [read post]
6 Sep 2011, 11:55 am
Author Rebecca Shafer, JD, President of Amaxx Risk Solutions, Inc. is a national expert in the field of workers compensation. [read post]
28 May 2014, 12:14 pm
The proposed rule available for review at http://www.gpo.gov/fdsys/pkg/FR-2014-05-28/pdf/2014-12245.pdf would establish a prior authorization process for certain durable medical equipment, prosthetics, orthotics, and supplies (DMEPOS) items that are frequently subject to unnecessary utilization and would add a contractor's decision regarding prior authorization of coverage of DMEPOS items to the list of actions that are not initial determinations and… [read post]
28 May 2014, 12:14 pm
The proposed rule available for review at http://www.gpo.gov/fdsys/pkg/FR-2014-05-28/pdf/2014-12245.pdf would establish a prior authorization process for certain durable medical equipment, prosthetics, orthotics, and supplies (DMEPOS) items that are frequently subject to unnecessary utilization and would add a contractor's decision regarding prior authorization of coverage of DMEPOS items to the list of actions that are not initial determinations and… [read post]
22 Mar 2018, 9:09 am
Aetna claims that Washington’s treating provider failed to timely provide medical records in response to Aetna’s pre-authorization review. [read post]
22 Mar 2018, 9:09 am
Aetna claims that Washington’s treating provider failed to timely provide medical records in response to Aetna’s pre-authorization review. [read post]
23 Mar 2021, 6:30 am
Author Michael Stack, CEO Amaxx LLC. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
24 Aug 2020, 10:00 pm
Morgan Lewis consultant Paul Ranson authored an article for European Pharmaceutical Review in which he explores the reasons behind the introduction of the EU Medical Device and In Vitro Diagnostic Devices Regulations. [read post]
