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Forum Diskusi Untuk Umum
Isu Terkini Seputar Farmakologi
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Info Obat dan Regulator Obat Dunia
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SafaLab, Inc. - 611233 - 02/18/2021
FDA
Oct 7, 2023
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0
Views
223
Oct 7, 2023
FDA
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FDA Roundup: October 6, 2023
FDA
Oct 7, 2023
Replies
0
Views
174
Oct 7, 2023
FDA
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Stimulant Use Disorders: Developing Drugs for Treatment
FDA
Oct 6, 2023
Replies
0
Views
137
Oct 6, 2023
FDA
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F
Remarks by Commissioner Califf at the Reagan Udall Foundation's Public Meeting on Strategies for Improving Public Understanding of FDA-Regulated Produ
FDA
Oct 6, 2023
Replies
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Views
231
Oct 6, 2023
FDA
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Risk of Invasive Disease in Preterm Infants Given Probiotics Formulated to Contain Live Bacteria or Yeast
FDA
Oct 6, 2023
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0
Views
216
Oct 6, 2023
FDA
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Initiatives at CDER
FDA
Oct 5, 2023
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0
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203
Oct 5, 2023
FDA
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Drug Trials Snapshot: BYLVAY
FDA
Oct 5, 2023
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0
Views
189
Oct 5, 2023
FDA
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F
Drug Trials Snapshot: LIVMARLI
FDA
Oct 5, 2023
Replies
0
Views
161
Oct 5, 2023
FDA
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FDA Launches Pilot Program to Help Further Accelerate Development of Rare Disease Therapies
FDA
Oct 5, 2023
Replies
0
Views
169
Oct 5, 2023
FDA
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The Bad Ad Program
FDA
Oct 5, 2023
Replies
0
Views
246
Oct 5, 2023
FDA
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FDA Roundup: October 3, 2023
FDA
Oct 4, 2023
Replies
0
Views
193
Oct 4, 2023
FDA
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Speech by Commissioner Robert M. Califf to the House of Medicine - 06/16/2023
FDA
Oct 4, 2023
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0
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148
Oct 4, 2023
FDA
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Remarks by Commissioner Robert M. Califf to the 2024 Global Summit in Regulatory Science - 09/26/2023
FDA
Oct 4, 2023
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184
Oct 4, 2023
FDA
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Remarks by Commissioner Califf to the Advancing Generic Drug Development: Translating Science to Approval Workshop - 09/13/2023
FDA
Oct 4, 2023
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203
Oct 4, 2023
FDA
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CPG Sec 100.200 FDA Jurisdiction Over Products Composed of Interstate Ingredients
FDA
Oct 4, 2023
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0
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159
Oct 4, 2023
FDA
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KVK-Tech, Inc. Issues Voluntary Nationwide Recall of One Lot of Betaxolol Tablets, USP 10 mg (Batch Number: 17853A) as a Precautionary Measure Due to
FDA
Oct 4, 2023
Replies
0
Views
136
Oct 4, 2023
FDA
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Common Issues with SEND Data Submitted for Safety Pharmacology Studies - 11/16/2023
FDA
Oct 4, 2023
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0
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182
Oct 4, 2023
FDA
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April - June 2023 | Potential Signals of Serious Risks/New Safety Information Identified by the FDA Adverse Event Reporting System (FAERS)
FDA
Oct 3, 2023
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0
Views
258
Oct 3, 2023
FDA
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Biomic Sciences Issues Voluntary Nationwide Recall of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray Products Due to Microbial Contamin
FDA
Oct 3, 2023
Replies
0
Views
136
Oct 3, 2023
FDA
F
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Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 25-28 September 2023, PRAC, 29/09/2023
EMA
Sep 30, 2023
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206
Sep 30, 2023
EMA
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