Recent changes
GovPing tracks 141 sources for this role out of 2,348 total sources on GovPing, covering Guidance, Enforcement, Rule, Notice, and Consultation instruments. There were 722 changes in the last 7 days.
Health Canada issued a Type I recall for nitrous oxide chargers sold by DOODELZ, Gold Whip, and Whip-it! brands without market authorization, while the UK VMD called for a Class II recall of Zoetis's Scabigard Suspension for cutaneous administration. FDA classified Draeger's Atlan A350 anesthesia workstations as a Class I recall due to potential piston ventilator failure, and Morovan recalled approximately 4,000 units of Gel Nail Polish Remover for methylene chloride and chloroform contamination.
IMIPAT Study - Parathyroid Tissue Injection - Medical University of Vienna
ClinicalTrials.gov registered a new interventional study (NCT07516990) conducted by the Medical University of Vienna investigating parathyroid tissue injection. The Phase 1 study is listed as actively recruiting and will evaluate safety and preliminary efficacy outcomes in human subjects.
Nomophobia study, Bahçeşehir University, recruiting
ClinicalTrials.gov registered a new observational study (NCT07518056) titled 'Nomophobia study' sponsored by Bahçeşehir University, Turkey. The study is currently recruiting participants and is listed as an observational study examining smartphone dependency (nomophobia). The registration makes the trial publicly accessible on ClinicalTrials.gov.
Cerebrospinal fluid kinetics of urolithin A study
NIH/NLM published a clinical trial registration on ClinicalTrials.gov (NCT07517913) for a study examining the cerebrospinal fluid pharmacokinetics of urolithin A in approximately 12 healthy participants. The single-center, open-label study will assess how urolithin A distributes into cerebrospinal fluid following oral administration.
Stroke rehab trial evaluating Environmental Mapping Tool
A stroke rehabilitation clinical trial has been registered on ClinicalTrials.gov (NCT07517120). The study evaluates an Environmental Mapping Tool as an intervention for stroke patients. The trial is now publicly listed, providing transparency on ongoing clinical research.
Metformin cream for psoriasis vulgaris, Cairo University trial
NIH/NLM registered a new clinical trial (NCT07516821) on ClinicalTrials.gov investigating topical metformin cream for treating psoriasis vulgaris. The Phase 2 study is sponsored by Cairo University in Egypt with an estimated enrollment of 60 participants. Results posting is required under FDAAA 801 for applicable trials.
Mass balance study LPM3770164 Huntington disease
The NIH National Library of Medicine registered ClinicalTrials.gov Identifier NCT07516899, a mass balance study evaluating LPM3770164 in patients with Huntington disease. Mass balance studies track drug absorption, distribution, metabolism, and excretion (ADME) to quantify material balance. The trial is listed in the US clinical trials registry.
Patient-derived organoids, breast cancer, chemotherapy resistance study
Patient-derived organoids, breast cancer, chemotherapy resistance study
ACE Surgical sutures recall due to unlicensed medical devices
Health Canada issued a Type II recall for ACE Surgical Supply® PGA Absorbable Sutures and Absorbable Gut Sutures distributed in Canada. BioHorizons Canada is conducting the recall because manufacturer ACE Surgical Supply Co. Inc. voluntarily ceased operations and discontinued its medical device licenses in Canada, resulting in unlicensed devices on the market. All lots of 17 affected catalogue numbers are subject to this recall. Healthcare providers who have distributed these sutures must cease use and contact the importer.
Nucletron B.V. Intrauterine Tube Recall - Tip Detachment
Health Canada issued a Type II medical device recall for Nucletron B.V. Intrauterine Tubes (catalog numbers 152019-00 through 126015-01) affecting 44 product lots. The recall addresses a safety concern where the tip of the 4mm diameter IU tube detached and remained within a patient during use. Healthcare providers should contact the manufacturer for additional information.
CMS Issues Guidance on New Medicaid and CHIP Funding Limits for Noncitizens
CMS issued guidance implementing new limits on federal Medicaid and CHIP matching funds for certain noncitizens under Public Law 119-21 Section 71109. States must implement system changes by October 1, 2026, including updates to eligibility systems, applications, verification, and claims processing. Exceptions exist for emergency medical conditions and coverage of lawfully residing children and pregnant women.
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737 changes in last 7 days
Latest high priority updates
142 official sources tracked
Frequently asked questions
What does this feed cover?
FDA warning letters, novel drug approvals, drug shortage notices, ICH guideline updates, USP notices, EMA news, DEA scheduling decisions, and TGA/WHO standards.
Who is this for?
Regulatory affairs professionals, pharmacovigilance teams, and medical affairs groups at pharma companies and CROs who need to track FDA and EMA actions.
How often is this updated?
GovPing checks source pages multiple times daily. FDA warning letters and drug approvals typically appear within hours of publication.
Does this cover EMA and international regulators?
Yes. We monitor the EMA, ICH, WHO, TGA (Australia), and other international health authorities alongside FDA.
How is this different from AgencyIQ?
AgencyIQ is a full FDA intelligence platform. GovPing is a free feed of the FDA, EMA, and ICH source pages where warning letters, approvals, drug shortages, and guidance are first published - AI-summarized with attention-level ratings on every change.
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