Basics of Cleaning Validation
Cleaning validation is a vital documentation that clearly indicates the process a pharma manufacturer follows to get rid of the residuals after producing specific drugs. This is done to avoid
BLOGS
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
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
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
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
Pharmaceutical Consultancy Services
With the thriving pharmaceutical sector in India, consultancy services play an indispensable role. With the constant evolution of regulatory landscapes, technological advancements, and market demands, pharmaceutical companies face numerous challenges.
What is Cleanroom Validation in Pharmaceuticals?
The term “cleanroom” is often found in a clean and controlled environment, especially in the pharmaceuticals, biotechnology, and electronics industries. Ensuring these environments maintain their required standards is crucial for
Turnkey Pharma Solutions
Introduction At PDVD Consultancy, we are experts in providing ready-to-use turnkey pharma solutions for the pharmaceutical and medical industry. We focus on planning, designing, validation, and documentation to ensure your
