Subscribe to Our Newsletter

Success! Now Check Your Email

To complete Subscribe, click the confirmation link in your inbox. If it doesn’t arrive within 3 minutes, check your spam folder.

Ok, Thanks

regulatory

A collection of 57 Posts

Trump Administration Unveils 100% Tariffs on Branded Drugs, Sparking Industry Alarm post image

Trump Administration Unveils 100% Tariffs on Branded Drugs, Sparking Industry Alarm

U.S. Announces 100% Tariff on Imported Patented Drugs, Poised to Reshape Global Pharmaceutical Supply Chains post image

U.S. Announces 100% Tariff on Imported Patented Drugs, Poised to Reshape Global Pharmaceutical Supply Chains

UK Minister: Higher Drug Prices Essential to Retain Pharma Investment and End Industry Feud post image

UK Minister: Higher Drug Prices Essential to Retain Pharma Investment and End Industry Feud

Yangtze River Pharma Unveils Positive Phase III Results for Insomnia Drug Fazamorexant, Submits NDA post image

Yangtze River Pharma Unveils Positive Phase III Results for Insomnia Drug Fazamorexant, Submits NDA

Senhwa Biosciences' CX-5461 Receives FDA IND Clearance for MYC-Driven Lymphoma Trial, Eyes Pan-Cancer Potential post image

Senhwa Biosciences' CX-5461 Receives FDA IND Clearance for MYC-Driven Lymphoma Trial, Eyes Pan-Cancer Potential

First Covid Pill That Prevents Infection After Exposure Awaits FDA Approval post image

First Covid Pill That Prevents Infection After Exposure Awaits FDA Approval

First Covid Pill That Prevents Infection After Exposure Awaits FDA Approval post image

First Covid Pill That Prevents Infection After Exposure Awaits FDA Approval

BBC xyz post image

BBC xyz

Clinical trial leads to FDA approval of drug for rare, deadly blood cancer post image

Clinical trial leads to FDA approval of drug for rare, deadly blood cancer

D3 Bio, Inc. Announces FDA Breakthrough Therapy Designation and Orphan Drug Designation for D3S-001 for the Treatment of Patients with KRAS G12C-Mutated Cancers post image

D3 Bio, Inc. Announces FDA Breakthrough Therapy Designation and Orphan Drug Designation for D3S-001 for the Treatment of Patients with KRAS G12C-Mutated Cancers

Celcuity to Initiate NDA Submission of Gedatolisib in PIK3CA Wild-Type Cohort in HR+/HER2- Advanced Breast Cancer Under FDA’s Real-Time Oncology Review Program post image

Celcuity to Initiate NDA Submission of Gedatolisib in PIK3CA Wild-Type Cohort in HR+/HER2- Advanced Breast Cancer Under FDA’s Real-Time Oncology Review Program

FDA Shift In Drug Approvals Halts Trial Of Second Skin Cancer Drug post image

FDA Shift In Drug Approvals Halts Trial Of Second Skin Cancer Drug