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Process Validation in Pharma Industry: A Complete Guide

The pharmaceutical industry demands rigorous oversight and control over its manufacturing processes to ensure the consistent quality of drugs and therapies. Among the most critical aspects of pharmaceutical production is process validation, a systematic approach that confirms a manufacturing process’s […]

Three Crucial Reasons for Selecting the Appropriate CDMO [E-Book]

Bringing a pharmaceutical product to market is no small feat. From research and development to commercialization, the path is filled with complex challenges. That’s why more pharmaceutical companies are turning to Contract Development and Manufacturing Organizations (CDMOs) to streamline their […]

Generic vs Brand Name Drugs: Key Differences Explained

When it comes to understanding prescription drugs, the distinction between a brand name drug and a generic drug is crucial. This guide will break down the core of the generic vs brand name drugs debate, focusing on generic names, brand […]

Bioequivalence studies: the key to a successful new generic

Generic drugs are a mainstay of patient treatment, making up more than 90% of drugs taken by patients in the US, and about two-thirds of those in Europe. As generics are, essentially, copies of innovative drugs whose safety and efficacy […]

Sterile Injectables: Key Considerations for Pharma Industry

Sterile injectables are a cornerstone of the pharmaceutical industry, playing a crucial role in patient care and the global healthcare system. These injectable drugs are essential for treating life-threatening diseases and managing chronic conditions. Given the nature of their application, […]

Process Analytical Technology: Enhancing Pharma Development

In the pharmaceutical industry, the demand for consistent product quality, regulatory compliance, and efficient manufacturing processes is higher than ever. As companies strive to meet these challenges, the adoption of advanced technologies has become crucial. One such innovation that has […]

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