IPP Bureau

Merck receives positive EU CHMP opinion for Keytruda as adjuvant treatment for  cell lung cancer
Merck receives positive EU CHMP opinion for Keytruda as adjuvant treatment for cell lung cancer

By IPP Bureau - September 18, 2023

Opinion granted based on positive disease-free survival results from the Phase 3 KEYNOTE-091 trial

Dr. Jitendra Singh flags off SMVD Narayana Healthcare TB Mukt Express
Dr. Jitendra Singh flags off SMVD Narayana Healthcare TB Mukt Express

By IPP Bureau - September 18, 2023

Public private partnership (PPP) with integrated strategy essential to achieve ‘TB Mukt Bharat’ by 2025

Minister Gadkari inaugurates the Robotic Urology Centre at UroKul, Pune
Minister Gadkari inaugurates the Robotic Urology Centre at UroKul, Pune

By IPP Bureau - September 16, 2023

UroKul, Pune is the largest centre to conduct reconstructive urology surgery outside USA and UK

Strides receives tentative USFDA approval for Dolutegravir/Lamivudine/Tenofovir Disproxil Fumurate tablets
Strides receives tentative USFDA approval for Dolutegravir/Lamivudine/Tenofovir Disproxil Fumurate tablets

By IPP Bureau - September 16, 2023

Approval of this product under the PEPFAR program completes Strides’ qualification to all major markets and donor programs including Global Fund and South Africa

AstraZeneca Pharma India appoints Praveen Akkinepally as Business Unit Head - Oncology
AstraZeneca Pharma India appoints Praveen Akkinepally as Business Unit Head - Oncology

By IPP Bureau - September 16, 2023

Currently, Praveen Akkinepally is the Head of Lung Cancer Commercialization, AstraZeneca Gaithersburg, MD, USA

Zydus receives final approval from USFDA for Norelgestromin and Ethinyl Estradiol Transdermal System
Zydus receives final approval from USFDA for Norelgestromin and Ethinyl Estradiol Transdermal System

By IPP Bureau - September 16, 2023

Norelgestromin and Ethinyl Estradiol Transdermal System, 150 mcg/35 mcg per day had annual sales of US $330 million in the United States

Strides receives tentative USFDA approval for Dolutegravir tablets
Strides receives tentative USFDA approval for Dolutegravir tablets

By IPP Bureau - September 15, 2023

The products will be manufactured at the company's facility in Bengaluru

Sun Pharma and Pharmazz ink agreement for introducing Tyvalzi in India
Sun Pharma and Pharmazz ink agreement for introducing Tyvalzi in India

By IPP Bureau - September 15, 2023

Sun Pharma is granted rights for marketing Sovateltide in India under the brand name Tyvalzi (Sovateltide)

Narayana Health unveils new brand identity
Narayana Health unveils new brand identity

By IPP Bureau - September 15, 2023

The new logo incorporates three beating hearts seamlessly & reinforces 'healthcare with a heart' into the Group's visual identity

SMi Systems secures UK patent for breakthrough single molecule imaging capabilities
SMi Systems secures UK patent for breakthrough single molecule imaging capabilities

By IPP Bureau - September 15, 2023

The super-resolution optical technology will accelerate discovery in biomedical research and transform in vitro diagnostics

Eye-Q launches Johnson and Johnson’s ELITA SILK procedure in India
Eye-Q launches Johnson and Johnson’s ELITA SILK procedure in India

By IPP Bureau - September 15, 2023

This advanced technology is specifically tailored for individuals with high power prescriptions, aiming to free the 18-35 age group from the reliance on eyeglasses

Ami Organics to supply additional API to Fermion
Ami Organics to supply additional API to Fermion

By IPP Bureau - September 15, 2023

The product is expected to start contributing meaningfully to the revenue from FY25

Cabinet approves foreign investment of up to Rs. 9,589 crore in Suven Pharmaceuticals
Cabinet approves foreign investment of up to Rs. 9,589 crore in Suven Pharmaceuticals

By IPP Bureau - September 14, 2023

The approval is for acquisition of up to 76.1% equity shares of Suven Pharmaceuticals by Berhyanda Limited

Bajaj Healthcare announces receipt of EIR from USFDA
Bajaj Healthcare announces receipt of EIR from USFDA

By IPP Bureau - September 14, 2023

The company has received the Establishment Inspection Report (EIR) from the USFDA for the Pre-Approval Inspection (PAI) at a manufacturing site situated at Savli, Vadodara, Gujarat, with Zero 483 observations

Celanese inks agreement with the Population Council to supply its VitalDose drug delivery platform
Celanese inks agreement with the Population Council to supply its VitalDose drug delivery platform

By IPP Bureau - September 14, 2023

The VitalDose Drug Delivery Platform has been used in patient-centric dose forms in women’s health for over two decades

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