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
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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
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
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.
Comprehensive Guide to Cleanroom Validation: Ensuring Contamination-Free Environments
Cleanrooms are critical in industries where even microscopic contaminants can compromise product quality, safety, or performance. From pharmaceutical manufacturing to semiconductor production and healthcare, cleanroom validation ensures these controlled environments
Why Planning a Pharmaceutical Facility Matters
Planning a pharmaceutical facility is crucial, especially in a country like India, where the pharmaceutical industry plays a significant role in the global supply chain. India is a leading exporter
