Thailand: Updated Dosage Limits for Drugs Containing Fa…
The Ministry of Public Health in Thailand has unveiled a draft notification outlining updated dosage limits for drugs containing fat-soluble…
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Pharma and Biotech
Proposed changes to the Pharmaceutical Advertising Advi…
Health Canada is currently scrutinizing a significant revamp of pharmaceutical advertising standards proposed by the Pharmaceutical Advertis…
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Pharma and Biotech
TGA Seeks Input: Adoption of International Scientific G…
The Therapeutic Goods Administration (TGA) Australia is actively seeking public input on the adoption of thirteen international scientific g…
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Pharma and Biotech
EU Draft Regulation: Banning BPA in Food Contact Materi…
The European Commission presents a draft regulation aiming to restrict the use of bisphenol A (BPA) and other bisphenols in materials and ar…
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Food and Nutrition
UK Government Report on Malaysian Palm Oil and EU’…
The UK Government has released an official report highlighting key findings and a positive verdict on the sustainability of Malaysian palm o…
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Food and Nutrition
Belgium Updates Authorized Plants in Food and Supplemen…
Belgium has published a significant update through an Order that revises the list of plants authorized in both food and food supplements. Th…
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Food and Nutrition
Ukraine Aligns Dietary Supplement Regulation with EU St…
Ukraine informs the World Trade Organization of a draft law aligning its dietary supplement regulation with EU standards. The proposal estab…
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Food and Nutrition
Thai FDA’s Proposed Draft Notification: Annual Sa…
Thai FDA proposes a draft Notification mandating annual safety reports for terminated or completed clinical research, aligning with Herbal P…
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Pharma and Biotech
FDA Guidance on Developing Chimeric Antigen Receptor (C…
The FDA’s latest guidance outlines crucial considerations for developing Chimeric Antigen Receptor (CAR) T cell products. Focused on s…
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Pharma and Biotech
US FDA Eases Informed Consent for Minimal Risk Clinical…
FDA Implements 21st Century Cures Act: Effective 30 days post-publication, ensuring rights and safety of human subjects. The final rule amen…
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Pharma and Biotech