CDMO Selection: The Ultimate Checklist
The biopharmaceutical industry has witnessed a significant surge in the number of therapeutic molecules in development, leading to a corresponding […]
The biopharmaceutical industry has witnessed a significant surge in the number of therapeutic molecules in development, leading to a corresponding […]
Achieving operational excellence in a Contract Development and Manufacturing Organization (CDMO) is crucial to ensure the quality and consistency of
Generic drugs play a crucial role in providing affordable healthcare options to millions of patients worldwide. One of the key
Using FDA Product Specific Guidances (PSGs) as a Trigger for Generic Drug Development Read Post »
The pharmaceutical industry, particularly the generic drug sector, faces significant challenges in adopting sustainable practices. As the world grapples with
How to Develop a Sustainable Generic Drug Development Strategy Read Post »
India has long been recognized as a significant player in the global pharmaceutical industry, particularly in the production of generic
India’s Growing Importance in Generic Drug API Manufacturing Read Post »
The pharmaceutical industry has undergone significant changes over the past decade, with a growing trend towards outsourcing key aspects of
The pharmaceutical and biotechnology industries are heavily regulated, and navigating these regulations can be a significant challenge for companies, especially
Generic drug development is a complex process that involves not only scientific and medical expertise but also adherence to strict
The Role of Scientific Expertise in Generic Drug Development Read Post »
Biosimilars have been transforming the pharmaceutical landscape by offering cost-effective alternatives to biologic drugs. As patents for these biologics expire,
Analyzing the impact of biosimilars on biologic drug manufacturing technologies Read Post »
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