IPP Bureau

Moderna announces promising efficacy results from mRNA flu vaccine trial
Moderna announces promising efficacy results from mRNA flu vaccine trial

By IPP Bureau - July 01, 2025

mRNA-1010 demonstrated superior relative vaccine efficacy

Pfizer strengthens AI collaboration with XtalPi to accelerate drug discovery
Pfizer strengthens AI collaboration with XtalPi to accelerate drug discovery

By IPP Bureau - July 01, 2025

The collaboration aims to enhance the accuracy of physics-based methods with AI models for optimising small molecule medicine discovery and development

PerkinElmer appoints Payal Agrawaal as MD - India & South Asia
PerkinElmer appoints Payal Agrawaal as MD - India & South Asia

By IPP Bureau - July 01, 2025

She will lead efforts to deepen regional market presence, foster innovation, and support scientific advancement across South Asia

Briefs: Lyfius Pharma and Aurobindo Pharma
Briefs: Lyfius Pharma and Aurobindo Pharma

By IPP Bureau - July 01, 2025

Lyfius Pharma restarts operations at Penicillin-G manufacturing facility

Indegene identified as leader in ISG's Provider Lens for life sciences digital services
Indegene identified as leader in ISG's Provider Lens for life sciences digital services

By IPP Bureau - July 01, 2025

ISG acknowledged Indegene's strengths in implementing holistic creative workflows, interoperability via robust integration with tech ecosystems

Biocon Biologics expands insulin access in Malaysia
Biocon Biologics expands insulin access in Malaysia

By IPP Bureau - June 30, 2025

Over 100 million cartridges of rh-insulin supplied to Malaysian health ministry; 345,000+ patients served

Fredun Pharmaceuticals acquires One Pet Stop to foray into pet care market
Fredun Pharmaceuticals acquires One Pet Stop to foray into pet care market

By IPP Bureau - June 30, 2025

The pet dog population alone is expected to increase from 21.4 million in 2019 to 51.5 million by 2028

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

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