What Does the USFDA Say About Metadata?
As the pharmaceutical industry moves toward digital records and electronic systems, the USFDA has clearly explained what…
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December 29, 2025
10 Habits That Prevent Errors in Documentation in Pharma
Documentation in pharma is not just about filling formats or completing records. It is about proving that…
December 22, 2025
Pharmaceutical Documentation: Documented But Not Performed
If documentation does not match reality, it defeats the entire purpose of GMP. This principle becomes extremely…
December 16, 2025
Understanding the Role of the Regulatory Affairs Department in Pharma
In every pharmaceutical company, the Regulatory Affairs (RA) Department plays a crucial role. It acts as the…
December 12, 2025
Soybean Casein Digest Medium (SCDM) and Its Role in Media Fills
In pharmaceutical microbiology, Soybean Casein Digest Medium (SCDM) is the most commonly used growth medium for media…
December 11, 2025
Risk-Based Approach in GMP
Good Manufacturing Practices (GMP) are the backbone of pharmaceutical quality. They ensure that every tablet, vial, and…
December 5, 2025
10 Pharmaceutical Companies in India
India’s pharmaceutical industry stands as a beacon of innovation and excellence, catering not only to the nation’s…
December 4, 2025
Lyophilization in Pharmaceuticals: Definition, Process, Importance, and Applications
Pharmaceutical companies widely use lyophilization to preserve sensitive drugs, vaccines, proteins, and biological materials. This advanced drying…
August 20, 2025
Top 5 Trends Shaping the Pharmaceutical Industry in 2025
The pharmaceutical industry is undergoing rapid transformation in 2025. The industry is driven by technological innovations, strategic…
August 19, 2025
What Kind of Entry Errors Are Acceptable in Pharma Documentation?
In the pharmaceutical industry, we do a lot of documentation in our day-to-day work, from entry logs…
August 18, 2025