IPP Bureau

Zydus receives warning letter from USFDA for Jarod injectables manufacturing facility
Zydus receives warning letter from USFDA for Jarod injectables manufacturing facility

By IPP Bureau - August 31, 2024

The company will take all necessary steps to work with USFDA towards earliest remediation of the above facility

Zydus receives USFDA final approval for Scopolamine Transdermal System 1 mg/3 days
Zydus receives USFDA final approval for Scopolamine Transdermal System 1 mg/3 days

By IPP Bureau - August 31, 2024

Thyrocare to acquire diagnostic and pathological services business of Vimta Labs
Thyrocare to acquire diagnostic and pathological services business of Vimta Labs

By IPP Bureau - August 31, 2024

Vimta Labs through its diagnostic and pathological services business has recorded a revenue of Rs. 30 crores during FY 2024 and Rs. 7 crores in Q1 FY 2025

DKSH partners with Hasten Biopharmaceutical’s growth in Thailand
DKSH partners with Hasten Biopharmaceutical’s growth in Thailand

By IPP Bureau - August 31, 2024

Indian doctor participates in Jordan’s first robotic radical hysterectomies
Indian doctor participates in Jordan’s first robotic radical hysterectomies

By IPP Bureau - August 31, 2024

Biocon Biologics secures market entry for Bmab 1200 in Europe, UK, Canada, and Japan
Biocon Biologics secures market entry for Bmab 1200 in Europe, UK, Canada, and Japan

By IPP Bureau - August 30, 2024

Biocon Biologics earlier announced a settlement agreement in the United States for a Bmab 1200 launch no later than February 22, 2025

Vaishali Pharma Ltd recommends 1:1 bonus issue and 1:5 stock split
Vaishali Pharma Ltd recommends 1:1 bonus issue and 1:5 stock split

By IPP Bureau - August 30, 2024

The company is making its mark through strategic initiatives, promising to become a significant presence in the evolving pharmaceutical sector

Natco Pharma announces submission of TABRECTA to USFDA
Natco Pharma announces submission of TABRECTA to USFDA

By IPP Bureau - August 30, 2024

TABRECTA is the brand of Novartis. Natco believes it is the first company to have filed a substantially-complete ANDA

Ayurvedic Whole System effective in Managing Rheumatoid Arthritis: Study
Ayurvedic Whole System effective in Managing Rheumatoid Arthritis: Study

By IPP Bureau - August 30, 2024

The study highlighted substantial improvements in key clinical parameters among RA patients who underwent AWS intervention

Suven Life Sciences announces FDA acceptance of investigational new drug
Suven Life Sciences announces FDA acceptance of investigational new drug

By IPP Bureau - August 30, 2024

First-in-human Phase-1 study will evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of SUVN-I6107 in healthy subjects

Bayer starts Phase III trial in non-small cell lung cancer
Bayer starts Phase III trial in non-small cell lung cancer

By IPP Bureau - August 30, 2024

First patient enrolled in the Phase III SOHO-02 trial of investigational agent BAY 2927088 in treatment-naïve patients with advanced NSCLC with HER2-activating mutations

Bayer awards incubator opportunity to Genvor
Bayer awards incubator opportunity to Genvor

By IPP Bureau - August 30, 2024

Critical resources will help Genvor to grow and scale biological crop protection products and innovative trait technologies

Lupin receives USFDA approval for Brimonidine Tartrate Ophthalmic Solution, 0.1%
Lupin receives USFDA approval for Brimonidine Tartrate Ophthalmic Solution, 0.1%

By IPP Bureau - August 28, 2024

Brimonidine Tartrate Ophthalmic Solution, 0.1% is an alpha adrenergic receptor agonist indicated for the reduction of elevated intraocular pressure

Aptar Closures introduces new lightweight 2? Disc Top Lite Closure for beauty and personal care
Aptar Closures introduces new lightweight 2? Disc Top Lite Closure for beauty and personal care

By IPP Bureau - August 28, 2024

The low-profile, 2” Disc Top Lite closure offers lighter weight combined with premium customization options

Zydus receives USFDA final approval for Amantadine ER capsules 68.5 mg
Zydus receives USFDA final approval for Amantadine ER capsules 68.5 mg

By IPP Bureau - August 28, 2024

Also received tentative approval for 137 mg

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