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NEWS & BLOGS
Blog: Blog2
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![FDA CDRH Social Media: Twitter, Facebook, and LinkedIn](https://static.wixstatic.com/media/22ea40_5b41beb99907477398a6ab312c098ca2~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_5b41beb99907477398a6ab312c098ca2~mv2.webp)
Provision Consulting Group
Jun 11, 20211 min read
FDA CDRH Social Media: Twitter, Facebook, and LinkedIn
The FDA's Center for Devices and Radiological Health uses social media to provide consumers, patients, caregivers, health care...
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![South Korea's Response to COVID-19](https://static.wixstatic.com/media/22ea40_e20ea9826a3b4fb583b8b642365c8519~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_e20ea9826a3b4fb583b8b642365c8519~mv2.webp)
Provision Consulting Group
Jun 9, 20211 min read
South Korea's Response to COVID-19
Picture from www.fda.gov/media/149334/download The FDA's Center for Devices and Radiological Health (CDRH) has issued a report that...
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![OTC Monograph Drug User Fee Program (OMUFA): Understanding FY 2021 User Fees Webinar](https://static.wixstatic.com/media/22ea40_fe331c6ea584451fa373a684b48d7360~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_fe331c6ea584451fa373a684b48d7360~mv2.webp)
Provision Consulting Group
May 28, 20211 min read
OTC Monograph Drug User Fee Program (OMUFA): Understanding FY 2021 User Fees Webinar
The questions regarding Over-The-Counter Monograph Drug User Fee from related establishments have been radically increasing. The FDA is...
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![FDA Warns Not Using Certain Needles With Safety Devices Made by HAIOU](https://static.wixstatic.com/media/22ea40_1e2cc3ca59244e3faa0ba8570e89b7ad~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_1e2cc3ca59244e3faa0ba8570e89b7ad~mv2.webp)
Provision Consulting Group
May 26, 20212 min read
FDA Warns Not Using Certain Needles With Safety Devices Made by HAIOU
The U.S. Food and Drug Administration on Thursday asked healthcare providers to stop using certain syringes and needles manufactured by...
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![FDA authorizes use of the Pfizer-BioNTech Covid Vaccine in adolescents ages 12 to 15](https://static.wixstatic.com/media/22ea40_54f64d72d61846beabb4bbf8453d1099~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_54f64d72d61846beabb4bbf8453d1099~mv2.webp)
Provision Consulting Group
May 19, 20212 min read
FDA authorizes use of the Pfizer-BioNTech Covid Vaccine in adolescents ages 12 to 15
On May 10, 2021, the U.S. Food and Drug Administration permits the emergency use of the Pfizer-BioNTech COVID-19 Vaccine in kids ages 12...
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![FDA Approves Treatment for Chronic Kidney Disease](https://static.wixstatic.com/media/22ea40_d02fcaf712b0465483bc0f829e4bb384~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_d02fcaf712b0465483bc0f829e4bb384~mv2.webp)
Provision Consulting Group
May 5, 20213 min read
FDA Approves Treatment for Chronic Kidney Disease
On April 3, 2021, the U.S. Food and Drug Administration approved Farxiga (dapagliflozin) oral tablets to reduce the risk of kidney...
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![Joint CDC and FDA Statement on Johnson & Johnson COVID-19 Vaccine](https://static.wixstatic.com/media/22ea40_c9ddf052b43c463ba9926e2821158baf~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_c9ddf052b43c463ba9926e2821158baf~mv2.webp)
Provision Consulting Group
Apr 15, 20212 min read
Joint CDC and FDA Statement on Johnson & Johnson COVID-19 Vaccine
The following statement is attributed to Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, and Dr....
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![New OTC Monograph User Fees for FY2021 is Announced](https://static.wixstatic.com/media/22ea40_c3f8718e9044452188c47d45efb79e0b~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_c3f8718e9044452188c47d45efb79e0b~mv2.webp)
Provision Consulting Group
Apr 7, 20213 min read
New OTC Monograph User Fees for FY2021 is Announced
BACKGROUND On March 27, 2020, "the Coronavirus Aid, Relief, and Economic Security Act" (CARES Act) was signed into law. Section 744M of...
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![FDA Alerts Public about Improper Use of Thermal Imaging Devices](https://static.wixstatic.com/media/22ea40_5693b34c53bb43489b3330be54788451~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_5693b34c53bb43489b3330be54788451~mv2.webp)
Provision Consulting Group
Mar 24, 20212 min read
FDA Alerts Public about Improper Use of Thermal Imaging Devices
The U.S. Food and Drug Administration alerted public of thermal imaging systems intended to measure human body temperature—also known as...
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![FDA Granted Marketing Authorization of First COVID-19 Diagnostic Test Using De Novo Review Pathway](https://static.wixstatic.com/media/22ea40_559cea44083a4fc3b503b3dad60c9321~mv2.jpg/v1/fill/w_454,h_256,fp_0.50_0.50,q_90,enc_auto/22ea40_559cea44083a4fc3b503b3dad60c9321~mv2.webp)
Provision Consulting Group
Mar 18, 20212 min read
FDA Granted Marketing Authorization of First COVID-19 Diagnostic Test Using De Novo Review Pathway
On March 17, 2021, the U.S Food and Drug Administration permits marketing authorization of the BioFire Respiratory Panel 2.1 (RP 2.1)....
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