Express Pharma

MARCH 12, 2025

The Indian Pharmaceutical Alliance (IPA) questions the reliance on the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) in the Ohio State University report titled, Are All Generic Drugs Created Equal? An Empirical Analysis of Generic Drug Manufacturing Location and Serious Drug Adverse Events.

Generic Medicine 66

Generic Medicine Process Improvement Dosage Pharmaceutical Manufacturing 66

Express Pharma

NOVEMBER 26, 2024

The 17th edition of CPHI & PMEC India, organised by Informa Markets in India opened its doors at the India Expo Centre, Greater Noida, Delhi-NCR, showcasing the robust potential of India’s pharmaceutical industry. and Rahul Deshpande, Sr. Group Director, Informa Markets in India, did the honours, amidst an august industry presence.

Packaging 105

Packaging Biosimilars Pharmaceutical Manufacturing Dosage 105

Express Pharma

JANUARY 17, 2025

As environmental concerns continue to intensify, the pressure on the pharmaceutical industry to reduce its overall environmental impact, particularly in final dosage forms, is growing proportionately. In March 2024, Lonza hosted its first digital Responsible Supplier Event which brought together more than 1,100 participants.

Dosage 104

Dosage Pharmaceutical Manufacturing Packaging Drug Development 104

Express Pharma

OCTOBER 7, 2024

On October 6, 2024, the Federation of Pharma Entrepreneurs (FOPE) and PharmaState Academy conducted Session 6 of the PULSE (Pharma Upgradation & Learning Series for Excellence) initiative, focusing on HVAC Systems and Qualification in pharmaceutical manufacturing. The session began with a keynote address by Thiru M.

Dosage 105

Dosage Pharmaceutical Manufacturing Packaging 105

Express Pharma

SEPTEMBER 24, 2024

Session Highlights: The event began with a keynote address by Manish Kapoor, State Drugs Controller of Himachal Pradesh, who emphasised the critical role that water systems play in maintaining pharmaceutical product quality. Express Pharma serves as the Media Partner, with Trillyum Consulting as the Knowledge Partner.

Dosage 101

Dosage Pharmaceutical Manufacturing 101

European Pharmaceutical Review

SEPTEMBER 29, 2022

The US Food and Drug Administration (FDA)’s Center for Drug Evaluation and Research (CDER) through the Office of Pharmaceutical Quality in 2021 embarked on an initiative to develop a framework for establishing a pharmaceutical manufacturing site quality rating system, the Quality management maturity (QMM) programme.

Nursing Homes 97

Nursing Homes Pharmaceutical Manufacturing Department of Veterans Affairs Dosage 97

pharmaphorum

JULY 28, 2022

While navigating changes has long been a challenge for the industry, the last two years’ events have made supply chain management significantly more difficult. The post How can the pharma industry navigate issues in the global supply chain to minimise drug shortages?

Diabetes 111

Diabetes Dosage Pharmaceutical Manufacturing Documentation 111