Flair Pharma The Knowledge Kit.
Pharmaceuticals Industrial revolution
The revolutionary approach to pharmaceutical development and manufacturing with Quality by Design (QBD). From systematic development processes to real-time monitoring and continuous improvement, QbD ensures the production of high-quality, safe, and effective drugs, transforming the industry’s landscape. Quality by Design (QbD) represents a paradigm shift in the pharmaceutical industry, emphasizing a systematic and science-based approach … Read more
In Generic vs Branded Medicines, Generic medicine refers to a pharmaceutical product that is equivalent to a brand-name (innovator) drug in terms of dosage, safety, strength, route of administration, quality, and intended use. The primary distinction between generic and brand-name drugs lies in their names and manufacturers. Here are key points to understand about generic … Read more
Transform your pharmaceutical formulation processes with our cutting-edge Apparent Bulk Density Apparatus. This sophisticated tool leverages precise measurement techniques, enabling accurate determination of apparent bulk density. In our plant, this apparatus serves as a technological cornerstone, facilitating the creation of pharmaceutical products with unparalleled precision and quality. Elevate your efficiency, ensure formulation consistency, and exceed … Read more
The acronym COBB stands for “Capacity (or Cobb) Absorbency Test,” named after its inventor, F.N. Cobb. The COBB test is used to measure the absorbency and resistance to liquid penetration of paper or paperboard materials. The Cobb sizing test provides valuable insights into the suitability of paper materials for specific applications, allowing manufacturers to select … Read more
Explore the critical importance of Laboratory Incident Reports in the Pharma Industry. Learn how incident documentation, analysis, and corrective actions ensure safety, quality, and regulatory compliance. Types of Laboratory Incidents: Laboratory incidents can vary in nature and severity, and it’s crucial to be aware of the common types to effectively prevent, address, and mitigate them. … Read more
The SOP for Entry and Exit Procedure for Grade C Area in an injectable pharmaceutical manufacturing plant is of paramount importance for ensuring the safety, quality, and integrity of the products being produced. Here are some key reasons why this procedure is crucial: Contamination Control: Grade C areas in pharmaceutical manufacturing are critical zones where … Read more
SOP for Entry and Exit for General Areas of pharmaceutical plants are critical to ensure the safety, security, and compliance of the facility. These procedures are in place to protect both the employees and the products being manufactured. The specifics may vary from one pharmaceutical plant to another, but here are some general guidelines and … Read more
