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.
Patent: Acetyl Glucosamine Improves Cognition
Patent: Acetyl Glucosamine Improves Cognition
Blueroot Health Expands Voluntary Recall of Vital Nutrients Aller-C Dietary Supplement Due to Undeclared Egg, Hazelnut, and Soy
Blueroot Health is expanding its voluntary recall of Vital Nutrients Aller-C dietary supplements to include all product from lot 25E04. The recall affects approximately 100 and 200 capsule bottles with lot numbers 25E04, 25E04-A, and 25E04-B, expiration date 05/27. The products were distributed nationwide from September 2025 through March 2026 and may contain undeclared egg, hazelnut, and soy allergens, posing a risk of serious or life-threatening allergic reactions.
Collagen Production Dietary Supplement Study
ClinicalTrials.gov has registered study NCT07521423, a clinical trial examining collagen production through dietary supplementation. The study focuses on understanding the effects of dietary supplements on collagen synthesis. Registration on ClinicalTrials.gov is required for certain clinical trials under federal law.
C-3002 Cervical Cancer Screening at CASCADE Sites, UNC Lineberger
NLM registered clinical trial NCT07520188 titled C-3002, a cervical cancer screening study conducted at CASCADE sites by UNC Lineberger. The registration provides trial identification, sponsor information, and study status for public transparency.
BXOS110 Injection Phase III Acute Ischaemic Stroke Trial
The National Library of Medicine registered a Phase III clinical trial (NCT07520565) evaluating BXOS110 Injection for acute ischaemic stroke. The trial appears to be investigating a novel therapeutic intervention. ClinicalTrials.gov serves as the public registry for clinical trials required under FDA regulations.
OCUL101 Neovascular AMD Phase II/III Trial
ClinicalTrials.gov registered Outlook Therapeutics' Phase II/III trial (NCT07520318) evaluating OCUL101 ophthalmic solution in treatment-naive subjects with neovascular age-related macular degeneration. The study will assess multiple endpoints including change from baseline in best-corrected visual acuity at 12 months.
MK-1045 Non-Hodgkin Lymphoma Phase 2 Trial, Merck
Merck registered a Phase 2 clinical trial (NCT07519772) evaluating MK-1045 for Non-Hodgkin Lymphoma on ClinicalTrials.gov. The trial is listed as a globally registered (GP) study. Clinical trial registration is required under FDAAA 801 for applicable trials and supports transparency in clinical research.
Bioequivalence Study Chiglitazar Metformin T2DM
The National Library of Medicine registered a new bioequivalence clinical trial on ClinicalTrials.gov. The study (NCT07519265) evaluates the bioequivalence of Chiglitazar and Metformin co-administration in patients with Type 2 Diabetes Mellitus (T2DM). The trial is listed as recruiting with an estimated enrollment of 36 participants at a single site in China.
HH-006 Chronic Hepatitis B Trial, Huahui Health
ClinicalTrials.gov registered the HH-006 clinical trial sponsored by Huahui Health, evaluating the safety and efficacy of an investigational treatment for chronic hepatitis B infection. The trial is now publicly listed with identifier NCT07519330, providing transparency on ongoing clinical research.
CAR 70-BCMA CAR-T Cells Relapsed Refractory Plasma Cell Neoplasms
ClinicalTrials.gov registered a new Phase 1/Phase 2 interventional study evaluating CAR 70-BCMA CAR-T cell therapy for adult patients with relapsed or refractory plasma cell neoplasms including multiple myeloma. The single-arm study will assess safety, tolerability, and efficacy of the BCMA-targeted autologous T-cell product. No compliance obligations are created by this registry entry.
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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.
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Regulatory affairs professionals, pharmacovigilance teams, and medical affairs groups at pharma companies and CROs who need to track FDA and EMA actions.
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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.
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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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