IPP Bureau

Lupin launches first generic version of Oracea in US
Lupin launches first generic version of Oracea in US

By IPP Bureau - April 10, 2024

Doxycycline Capsules, 40 mg is indicated for the treatment of only inflammatory lesions (papules and pustules) of rosacea in adult patients

Shivalik Rasayan’s API facility gets 7 observations from USFDA
Shivalik Rasayan’s API facility gets 7 observations from USFDA

By IPP Bureau - April 10, 2024

These observations are procedural in nature and will be responded within the stipulated time

President Murmu to inaugurate homeopathic symposium on World Homoeopathy Day 2024
President Murmu to inaugurate homeopathic symposium on World Homoeopathy Day 2024

By IPP Bureau - April 10, 2024

Empowering Research, Enhancing Proficiency is the theme of this year’s Homoeopathic Symposium

SPARC announces results from planned interim analysis of PROSEEK Study
SPARC announces results from planned interim analysis of PROSEEK Study

By IPP Bureau - April 10, 2024

Eugia Steriles gets 3 observations from USFDA for injectable facility
Eugia Steriles gets 3 observations from USFDA for injectable facility

By IPP Bureau - April 07, 2024

The observations are procedural in nature and will be responded to within the stipulated time

Bayer and Dr. Reddy's sign marketing and distribution agreement for second brand of Vericiguat in India
Bayer and Dr. Reddy's sign marketing and distribution agreement for second brand of Vericiguat in India

By IPP Bureau - April 07, 2024

Vericiguat works on a pathway not currently targeted by existing heart failure treatments

Gland Pharma receives USFDA approval for Eribulin Mesylate Injection
Gland Pharma receives USFDA approval for Eribulin Mesylate Injection

By IPP Bureau - April 07, 2024

The Product is expected to be the first generic approval on the market

Pluss unveils Celsure XL VIP pallets
Pluss unveils Celsure XL VIP pallets

By IPP Bureau - April 07, 2024

A game changing solution for the pharmaceutical industry

Wacker and Pantherna intensify collaboration in the development and production of mRNA biopharmaceuticals
Wacker and Pantherna intensify collaboration in the development and production of mRNA biopharmaceuticals

By IPP Bureau - April 07, 2024

Wacker Biotech is a CDMO for the GMP-compliant production of active ingredients for the pharmaceutical industry

LANXESS showcases extensive portfolio for the cosmetics industry at in-cosmetics Global
LANXESS showcases extensive portfolio for the cosmetics industry at in-cosmetics Global

By IPP Bureau - April 07, 2024

Highly effective preservation solutions ensuring the safety and protection of personal care products

Cipla Patalganga facility gets 6 USFDA observations
Cipla Patalganga facility gets 6 USFDA observations

By IPP Bureau - April 07, 2024

The regulator carried out a routine current Good Manufacturing Practices (cGMP) inspection from March 28 to April 4.

USFDA approves Bristol Myers and 2seventy bio’s Abecma for triple-class exposed multiple myeloma
USFDA approves Bristol Myers and 2seventy bio’s Abecma for triple-class exposed multiple myeloma

By IPP Bureau - April 06, 2024

Abecma tripled progression-free survival compared to standard regimens in the Phase 3 KarMMa-3 trial

Enhertu approved in the US as first tumour-agnostic HER2-directed therapy
Enhertu approved in the US as first tumour-agnostic HER2-directed therapy

By IPP Bureau - April 06, 2024

Enhertu now has five approved indications with the latest in HER2-expressing (IHC 3+) metastatic cancers

Imfinzi significantly improved overall survival and progression-free survival in ADRIATIC Phase III trial
Imfinzi significantly improved overall survival and progression-free survival in ADRIATIC Phase III trial

By IPP Bureau - April 06, 2024

First and only immunotherapy to demonstrate survival benefit in this setting in a global Phase III trial

Pfizer’s Velsipity UK approval will raise competition in ulcerative colitis market, says GlobalData
Pfizer’s Velsipity UK approval will raise competition in ulcerative colitis market, says GlobalData

By IPP Bureau - April 06, 2024

The approval marks a significant milestone for the American pharmaceutical company in the field of UC

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