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Installation Qualification process in pharmaceutical manufacturing

Installation Qualification in Pharmaceuticals

In pharmaceutical manufacturing, equipment earns credibility the hard way. Novelty and sophistication alone do not grant permission to participate in production. Before a single control is engaged or a parameter

GMP vs cGMP comparison for pharma facilities

Difference between cGMP and GMP

A practical guide for pharmaceutical facilities that cannot afford guesswork Walk into any pharmaceutical manufacturing plant at 7:00 a.m. sharp, and you’ll notice something almost theatrical. Stainless steel gleams like

Pharmaceutical Manufacturing Facility Design

Designing a pharmaceutical manufacturing facility is far more complex than constructing a conventional industrial building. From regulatory compliance and process optimization to future scalability and contamination control, every decision directly

Good Documentation Practices (GDP) in Pharmaceuticals

From simple over-the-counter (OTC) medicines to complex productions like vaccines, medical devices, and nutritional supplements, a specific quality, efficacy, and safety are more than mandatory. Dropping a ball on any

Validation Program in Pharmaceutical Industries

Pharmaceutical entities heavily depend upon quality assurance. Here, dependable validation becomes more than mandatory to ensure that every form of drug, including capsules, pills, syrups, and IVs, is produced in

Current Good Manufacturing Practices — cGMP in Pharmaceutical Industries Current Good Manufacturing Practices

With consistently advancing technologies, medical inventions, pharma space has also leaped drastically. With growth also rises the need to regulate and monitor. That’s why we need GMP (Good Manufacturing Practice)

Importance of Validation in Pharmaceuticals

Pharmaceuticals, a very crucial sector for the survival of humankind and one that is very close to the healthcare sector, depend heavily on quality control. While it is mandatory, it

What’s the Difference Between GMP and GDP in Facility Design?

Regulatory standards for the pharmaceutical space are a wide territory. It includes something as noticeable as Temperature and Humidity Control, to as intricate as Microbiological Testing. The measures to ensure

Pharma facility design for safety and efficiency

What Should You Know About Pharmaceutical Facility Design?

The trajectory of pharmaceutical success does not solely rely upon clinical data or laboratory triumphs. The silent milestones often lie in the design and construction of the facility, where ideas

Pharmacovigilance and regulatory compliance workflow

Significance of Pharmacovigilance in the Pharma Industry

Medicines, their quality, effectiveness, and the perfect amount of drugs within them are thanks to the regulations and dos and don’ts of the pharma industry. Sometimes, even after making sure

In Process Quality Control: IPQC in Pharmaceutical Industry

The pharma industry is one of the most quality-sensitive industries. A very important part of quality assurance for pharma products is Good Manufacturing Practices (GMP), and IPQC is a critical

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

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

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

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

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.