Regulatorische Updates
Regulatorische Entwicklungen von FDA, EMA, TGA und weltweit
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
Potential Pulmonary Aspiration Risk with GLP-1 Agonists During Anaesthesia
Healthcare professionals warned of pulmonary aspiration risk in patients on GLP-1 or dual GIP/GLP-1 agonists undergoing general anaesthesia or deep sedation.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
CHM Removes Specialist Review for Men Already on Valproate, Retains for New Patients Under 55
The Commission on Human Medicines says men already taking valproate no longer need a specialist review, while the requirement stays for patients under 55 starting the drug.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
PMCPA Rebukes Alnylam After Pfizer Complaint; UK Watchdog Overturns
Pfizer complained about Alnylam’s promotional activities at a cardiology congress, prompting the PMCPA to criticize the biotech, but the UK marketing watchdog later reversed its harshest finding on appeal.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
US Launches Probe into Germany's Alleged Underpayment for New Medicines
The United States is investigating Germany over what the USTR calls persistent underpayment for new pharmaceuticals amid German drug‑spending reforms.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
Korean Pharmacists Hold 273rd Relay Protest for Herbal Pharmacist Licensing Reform
The Korean Pharmaceutical Association and regional pharmacy societies held the 273rd relay protest in front of the Blue House, urging the government and parliament to amend the Pharmacy Act and define clear licensing for herbal pharmacists.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
MFDS proposes label changes for 134 dapagliflozin/metformin combo products
South Korea's MFDS has drafted an amendment to approval conditions for 134 dapagliflozin‑metformin combination drugs, seeking public comments to unify efficacy, dosage and safety guidance.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
FDA Approves ANDA077168 for Fluticasone Propionate Topical Ointment by Cosette Pharmaceuticals
The FDA has approved ANDA077168 for a prescription topical ointment containing 0.005% fluticasone propionate, manufactured by Cosette Pharmaceuticals.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
FDA Approves ANDA076877 for Gabapentin Tablets (Discontinued)
FDA approved ANDA076877 for gabapentin 600mg and 800mg oral tablets submitted by Senores Pharms; both products are listed as discontinued.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
FDA Grants ANDA Approval for Ciprofloxacin Hydrochloride Tablets (ANDA 076593)
The FDA approved generic ciprofloxacin hydrochloride tablets (250 mg, 500 mg, 750 mg) under ANDA 076593, sponsored by Aiping Pharm and manufactured by Westminster Pharmaceuticals.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
Recall: Ifosfamide IV Vials Not Refrigerated at Amerisource Bergen Distribution Centers
Certain vials of Ifosfamide IV were found to have been stored without refrigeration at Amerisource Bergen distribution centers, prompting a recall.
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
FDA Recalls Product Due to CGMP Deviations
The FDA has initiated a recall of a product because of deviations from current Good Manufacturing Practices (CGMP).
Regulatorische Updates
24. Aug. 2026•1 Min. Lesezeit
MHRA Publishes Summary of Recent Medicine and Device Safety Letters
The UK Medicines and Healthcare products Regulatory Agency (MHRA) released a summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.