Skip to content

BLOGS

GMP documentation

Different Types of GMP Documentation Used In the Pharma Industry

In the pharmaceutical industry, the importance of Good Manufacturing Practices (GMP) cannot be overstated. The pharmaceutical industry, like any other healthcare-related industry, must adhere to strict compliance standards that ensure
Continue Reading
guide to ISO starndard for clean room vadlidation

What is the ISO Standard for Clean Room Validation?

Multiple sectors are vulnerable to contaminants. To encourage industries with precision in cleanlines, the ISO standard for cleanroom validation is introduced. Sectors like pharmaceuticals, biotech, and aerospace, where even a
Continue Reading
pharmaceutical facility designing

Common Mistakes in Pharmaceutical Facility Design and How to Avoid

Developing a pharmaceutical facility while ensuring the smooth running of operations and documentation is no easy task. It is a group of a handful of heavy tasks. We, at PDVD
Continue Reading
schedule M guidelines

What are Schedule M Guidelines?

What are Revised Schedule M Guidelines? India’s pharmaceutical industry, a global leader in generic drug production, has taken a significant step toward reinforcing quality standards with the introduction of the
Continue Reading
pharmaceutical documentation

Top 5 Pitfalls in Pharmaceutical Documentation (How to Avoid Them)

Pharmaceutical documentation is the backbone of regulatory compliance, product quality, and patient safety. Yet, even seasoned professionals encounter pitfalls that can lead to costly delays, regulatory citations, or compromised data
Continue Reading
pharmaceutical API plant

What is a Pharmaceutical API Plant and How Does it Work?

The pharmaceutical areas deal in precision, innovation, and relentless commitment to quality. One crucial contributor to this complicated ecosystem is a pharmaceutical API plant, where the magic of medicine initiates.
Continue Reading