Flair Pharma The Knowledge Kit.
Pharmaceuticals Industrial revolution
Bulk Packing & Counting Line for tablets/capsules: In the Pharmaceutical industry, Bottle Packing lines are commonly used for packing tablets and capsules. Various types of plastic bottles are used for drug packing so that the Bottle Packing line for tablets or capsules. The major process that is used in Bottle Packing Line is as below: … Read more
The Strip Packing machine is widely used equipment in pharmaceutical industries mostly to pack tablet capsules & pills in aluminum foil and make them safe & ready to distribute in the market, and with the help of Automation, High-speed Strip Packaging machines are handled by a wide range of tablets and capsules up to 2500 … Read more
A Tablet coating machine is used to provide a coating over uncoated tablets, which protects them from environmental moisture, and chemical degradation and masks the bitter taste of the drug, etc. Also, the Coating machine shall have provision for film coating (Aqueous / Non-Aqueous) and sugar coating with interchangeable type coating pans of different capacities. … Read more
Tablet Compression Machine or tablet press is the equipment that is widely used in every pharmaceutical formulation plant to make an oral solid dosage form (tablet form) of the drug. In the below article, we discussed the working principles, major components, and all technical details which are considered by the formulation plant. … Read more
Computer System Validation (CSV): In pharmaceutical industries, every manufacturing plant will run its system, machines, and product in self-driven mode ie. “Automation” and these systems have critical software, computerized controls, and measurements. As a result, regulatory authorities make it mandatory to validate and standardize computer systems in accordance with their standards. So that the worldwide … Read more
The FACTORY ACCEPTANCE TEST (FAT) document is the major document and part of the master validation plan in every pharmaceutical organization. It’s a process that is performed at the OEM factory/Site, a pre-check before the delivery of the machine to the pharma organization site. Below details of are factory acceptance test examples. OBJECTIVE & … Read more
Installation Qualification (IQ) document is a very important document in the VMP (Validation Master Plan) of every pharmaceutical organization. Installation qualification is a documentation process, that will ensure an equipment/machine or instrument has been delivered, installed, and configured at your site in accordance with manufacturer standards and approved with the installation checklist as guided by … Read more
Design Qualification (DQ) is a widely used document in every pharma industry. The DQ is a key input to the commissioning and qualifications as per VMP. After OEM understood the user requirement specification (URS), his team generate the design qualification (DQ) document & submit this to the pharma organization. This also leads to verification that … Read more
URS is the most important document of every pharmaceutical industry which include all information about the particular system or equipment/Machine. URS is the 1st pillar of the VMP Validation Master Plan. URS has all information like Capacity, technology requirements, technical requirements, operational requirements, all types of specifications, etc. In the pharmaceutical formulation plant, the prime … Read more
To sell the pharmaceutical product in any country, your manufacturing plant will inspect by the respective country’s regulators’ authority. Then these regulators’ authorities provide an Approval certification to the manufacturing plant for a certain time period. Then formulation plant authorizes to manufacture the pharmaceutical product for the respective country. Market name Regulatory authority Name … Read more