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Home » Topics » Regulatory front

Regulatory front
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Regulatory front for Jan. 25, 2021

Jan. 25, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Telehealth bill resurfaces in 117th Congress; OIG includes telehealth in FY 2021 workplan.
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Regulatory front for Jan. 22, 2021

Jan. 22, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed urges administration to communicate on DPA; FDA posts third-party report for Q1, FY 2021.
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Regulatory front for Jan. 21, 2021

Jan. 21, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Hahn out, Woodcock in as acting FDA commissioner; White House orders regulatory freeze.
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Regulatory front for Jan. 20, 2021

Jan. 20, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CMS, OIG differ on CERT program.
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Regulatory front for Jan. 20, 2021

Jan. 20, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Jan. 19, 2021

Jan. 19, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA to hold webinar for respirator policy.
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Regulatory front for Jan. 19, 2021

Jan. 19, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Jan. 15, 2021

Jan. 15, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CMS wraps up prior authorization rule; ITC finds no violation of Section 337.
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Regulatory front for Jan. 15, 2021

Jan. 15, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory front for Jan. 14, 2021

Jan. 14, 2021
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: HHS examines device classification process at FDA; NIH offers NGS system for SARS-CoV-2; FDA issues pandemic policy for coagulation systems.
Read More
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