Unveiling Mounjaro (Tirzepatide): A Potential Breakthrough in Diabetes Treatment

Mounjaro (Tirzepatide): A diabetes and weight loss drug Introduction: Diabetes, a chronic metabolic disorder affecting millions of people worldwide, poses severe health challenges and demands effective treatment as soon as possible. The global prevalence of diabetes has been steadily rising highlighting the urgent need for innovative therapeutic interventions. Fortunately, medical advancements have introduced a promising […]

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mounjaro, tirzepatide, weight-loss

What is Aduhelm aducanumab drug? | Side effects, Cost, and benefits of Aducanumab

Introduction: Aduhelm aducanumab drug is a medication in an injectable form that contains Aducanumab 170mg /1.7 ml (100mg/ml). It is used to treat Alzheimer’s disease. Aducanumab is a monoclonal antibody. It targets the amyloid protein that clumps into plaques in the brain of Alzheimer’s patients. It is considered the main cause of disease. The US

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aducanumab, aduhelm, Alzheimer's-Disease

ICH Guidelines

What are the ICH Guidelines? ICH stands for International Conference on Harmonisation, which is a committee that provides a framework for the stability of products in the pharmaceutical industry. ICH guidelines are adopted by every country in the world for the stability conditions and testing of products. ICH guidance is also used for product development

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Wegovy [Semaglutide] new weight loss drug approved by FDA

U.S. Food and Drug Administration approved the most awaited obesity drug Wegovy which contains Semaglutide 2.4 mg in injection form. As per the U.S. FDA, the medicine is advised once a week for chronic weight loss management. In patients with high B.P., Diabetes type 2, and high cholesterol, this drug is recommended with physical activity.

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approved, common side effects, contradictions, dosage, drug, fda, semaglutide, wegovy, weight loss

MHRA guidelines for quality manufacturers of pharmaceutical formulations

The Medicines and Healthcare Products Regulatory Agency (MHRA) is a government agency in the United Kingdom. MHRA’s prime role is to regulate medicines, medical devices, and blood components for transfusion in the UK. MHRA guidelines are very important recommendations for any drug-related activity in the United Kingdom. It is a branch of the Department of

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Inida, MHRA guidelines, pharma

USFDA inspection checklist for a pharmaceutical facility

USFDA approval is a big milestone for any pharmaceutical manufacturing facility. If you are looking to export medicines to the US then you must have your facility approved by the USFDA. A pharma company can only sell direct products in the US market if they have got approval from the USFDA department. Every drug manufacturer

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