IPP Bureau

Briefs: Neuland Laboratories and Granules India
Briefs: Neuland Laboratories and Granules India

By IPP Bureau - June 29, 2025

Granules India receives 1 observation from USFDA for Chantilly facility

Alembic announces USFDA final approval for single-dose vials
Alembic announces USFDA final approval for single-dose vials

By IPP Bureau - June 29, 2025

Doxorubicin Hydrochloride Liposome Injection is indicated for the treatment of Ovarian Cancer, AIDS-Related Kaposi's Sarcoma, and Multiple Myeloma

Sartorius expands manufacturing and R&D capacities for bioprocess solutions in France
Sartorius expands manufacturing and R&D capacities for bioprocess solutions in France

By IPP Bureau - June 29, 2025

Extended lab space for product development, customer demos, and training

Zambon launches intravenous formulation of Fluimucil
Zambon launches intravenous formulation of Fluimucil

By IPP Bureau - June 29, 2025

The approval in China is supported by a robust local clinical development program confirming the drug’s safety, tolerability, and efficacy profile

Torrent Pharma to acquire KKR’s stake in JB Pharma for Rs. 25,689 Cr
Torrent Pharma to acquire KKR’s stake in JB Pharma for Rs. 25,689 Cr

By IPP Bureau - June 29, 2025

Acquisition to be followed by merger; strengthens Torrent’s IPM market presence

Shukra Pharmaceuticals receives LoA from RMSCL
Shukra Pharmaceuticals receives LoA from RMSCL

By IPP Bureau - June 28, 2025

The company has been awarded a contract for the supply of essential pharmaceutical formulations to government health institutions across Rajasthan

European Commission approves Eylea 8 mg with extended 6-month treatment interval for nAMD and visual impairment due to DME
European Commission approves Eylea 8 mg with extended 6-month treatment interval for nAMD and visual impairment due to DME

By IPP Bureau - June 28, 2025

Eylea 8 mg is the first and only anti-vascular endothelial growth factor (VEGF) treatment in the EU with treatment intervals of up to 6 months for both patients with nAMD and DME

FDA approves removal of REMS programs within Bristol Myers Squibb’s cell therapy labels
FDA approves removal of REMS programs within Bristol Myers Squibb’s cell therapy labels

By IPP Bureau - June 28, 2025

Label updates reflect growing body of real-world evidence and regulatory confidence in the safety profile of the class of CD19- and BCMA-directed autologous CAR T cell therapies, reinforcing efforts to increase equitable access

EMA starts review of sodium oxybate in alcohol dependence
EMA starts review of sodium oxybate in alcohol dependence

By IPP Bureau - June 28, 2025

Review will evaluate effectiveness in treating alcohol withdrawal syndrome and supporting abstinence, as well as measures to mitigate risk of abuse

Biocon Biologics receives Health Canada approval for Yesafili
Biocon Biologics receives Health Canada approval for Yesafili

By IPP Bureau - June 27, 2025

The approval is based on a comprehensive package of analytical, nonclinical, and clinical data

Star Health Insurance partners with Medi Assist to transform claims through AI and Digital Innovation
Star Health Insurance partners with Medi Assist to transform claims through AI and Digital Innovation

By IPP Bureau - June 27, 2025

Star Health Insurance is modernising its claims ecosystem to be future-ready

SMS Pharmaceuticals completes USFDA inspection at Central Laboratory Analytical Services
SMS Pharmaceuticals completes USFDA inspection at Central Laboratory Analytical Services

By IPP Bureau - June 27, 2025

The inspection concluded with zero Form 483 observations

Lupin launches Prucalopride tablets in US
Lupin launches Prucalopride tablets in US

By IPP Bureau - June 27, 2025

Prucalopride Tablets are bioequivalent to Motegrity Tablets, 1 mg and 2 mg, of Takeda Pharmaceuticals USA

Philogen withdraws marketing authorization application for Nidlegy in EU
Philogen withdraws marketing authorization application for Nidlegy in EU

By IPP Bureau - June 26, 2025

The company's decision to withdraw the MAA was due to the timing of the availability of Chemistry Manufacturing and Controls

Dr. Lal PathLabs strengthens its genomics capabilities with Illumina's NovaSeq X Series
Dr. Lal PathLabs strengthens its genomics capabilities with Illumina's NovaSeq X Series

By IPP Bureau - June 26, 2025

The NovaSeq X system features Illumina's cutting-edge XLEAP-SBS chemistry, offering unmatched throughput, accuracy, and sustainability

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