法规动态
FDA、EMA、TGA 及全球法规动态
法规动态
2026年8月25日•1 分钟阅读
MHRA Issues Guidance for Reporting Adverse Incidents with Diabetes Management Equipment
The MHRA urges healthcare professionals to support new guidance on reporting suspected adverse incidents related to insulin pumps and CGM devices.
法规动态
2026年8月25日•1 分钟阅读
MHRA reminds HCPs to discuss GLP‑1RA side effects with patients
Healthcare professionals should inform patients of common and serious side effects of GLP‑1 receptor agonists.
法规动态
2026年8月24日•1 分钟阅读
FDA Recall: Foreign Substances and Heavy Metals Detected in Product
FDA has recalled a product after routine stability testing revealed visible foreign substances, including heavy metals such as chromium and titanium, and inactive components.
法规动态
2026年8月24日•1 分钟阅读
MHRA Issues October 2024 Drug Safety Update to Healthcare Professionals
The MHRA released a summary of letters and notifications regarding medicines and medical devices sent to healthcare professionals in October 2024.
法规动态
2026年8月24日•1 分钟阅读
MHRA Publishes Summary of Recent Medicine and Device Safety Notices
The MHRA has released a summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
法规动态
2026年8月24日•1 分钟阅读
FDA Approves ANDA078070 for Valacyclovir Hydrochloride Tablets by Pharmobedient
The FDA approved application ANDA078070 submitted by Pharmobedient for oral valacyclovir hydrochloride tablets (500 mg and 1 g equivalents). Both products are listed as discontinued.
法规动态
2026年8月24日•1 分钟阅读
FDA Approves Padagis Israel’s Desoximetasone 0.25% Topical Ointment (ANDA077770)
The FDA granted approval (ANDA077770) for Padagis Israel’s prescription topical ointment containing 0.25% desoximetasone.
法规动态
2026年8月24日•1 分钟阅读
FDA Approves Ondansetron Injectable (ANDA077473)
The FDA has approved ANDA077473 for ondansetron injectable, manufactured by Hospira, for intramuscular and intravenous use.
法规动态
2026年8月24日•1 分钟阅读
FDA Identifies GMP Violations Affecting Sterility Assurance
An FDA inspection uncovered GMP violations that may compromise product sterility and quality, prompting a recall.
法规动态
2026年8月24日•1 分钟阅读
FDA Recall: CGMP Deviations Due to Intermittent Temperature Excursions
The FDA has issued a recall citing CGMP deviations caused by intermittent temperature excursions during storage.
法规动态
2026年8月24日•1 分钟阅读
Label Mix-up: Amantadine Capsules Contain Cyclobenzaprine Tablets
FDA recall (D-1035-2017) reports cartons labeled as Amantadine HCl 100 mg capsules actually contain Cyclobenzaprine HCl 5 mg tablets due to a labeling error.
法规动态
2026年8月24日•1 分钟阅读
MHRA Issues Summary of Recent Medicine and Device Safety Letters (Dec 2024)
The MHRA released a summary of letters and notifications sent to healthcare professionals about medicines and medical devices in December 2024.