Tag: Pharmaceutical manufacturing

At the end of 2023, 323 drugs were in active shortage in the US, the highest number since recordkeeping began in 2001, highlighting the urgent and complex problem of **why are so many prescription drugs out of stock**. The reasons behind this scarcity are multifaceted, involving a web of manufacturing, economic, and logistical challenges that disrupt the global pharmaceutical supply chain.

According to the FDA, a Drug Master File (DMF) is a confidential submission providing detailed information about a drug's manufacturing, processing, or packaging. Its primary purpose is to safeguard a company's confidential proprietary information while providing regulatory agencies with necessary data for drug application evaluation.

In the European Union, no medicinal product can be released for sale without a Qualified Person's certification. So, who is a qualified person for Directive 2001 83 EC, and what stringent criteria must they meet to uphold public health standards and ensure pharmaceutical quality?

Oral solid dosage forms like tablets and capsules account for a significant portion of approved medications, with tablets making up 64.5% and capsules 22.7% of immediate-release solids [1.8.1]. While popular for their high bioavailability, it's important to ask: **what are the disadvantages of soft gel capsules?**

As one of the top 10 generic pharmaceutical companies in the world, Aurobindo Pharma plays a significant role in global healthcare [1.6.2]. But a common point of confusion is what is the drug Aurobindo used for? The answer is that Aurobindo is a manufacturer, not a single drug.

As one of India's largest privately-held pharmaceutical companies, Cadila Pharmaceuticals develops and manufactures over 850 products [1.6.3]. So, when asking 'What is the use of Cadila Tablet?', the answer depends entirely on which specific medication from their vast portfolio you have.

With members from over 160 countries, the International Organization for Standardization (ISO) develops and publishes globally recognized standards. In the highly regulated world of pharmaceuticals, understanding **what does ISO stand for in pharma?** is crucial for ensuring the quality, safety, and efficiency of products that ultimately reach patients. While its primary meaning relates to quality standards, the term 'iso' has also emerged in a completely different context as a street drug.

With the US market alone accounting for a significant share of the oral solid dosage pharmaceutical market, understanding common industry terms is crucial. In the pharmaceutical world, OSD means Oral Solid Dosage, and it is a term used for a wide range of medications, including tablets and capsules. This guide will explore what OSD entails, its key benefits, and how these vital drug forms are created.

In 2015, the Nobel Prize was awarded for discoveries related to avermectin and ivermectin, highlighting the drug's immense global health impact. Understanding how you make ivermectin reveals a complex, multi-stage process far beyond the scope of a home laboratory, involving specialized microbial fermentation and chemical synthesis.

Over 70% of the manufacturing facilities for active pharmaceutical ingredients (APIs) supplying the U.S. are located overseas, primarily in India and China [1.2.1, 1.3.1]. This fact highlights the central question: **where does America get most of its pharmaceuticals**? The answer is a complex global network.