KM Production Unit
KM At A Glance
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Research and Development Section
KM continues to carry out research on botanicals, minerals and their therapeutic effects on various diseases. All the information is recorded to prepare the formulation under the guidance of head research and development. The product is tested according to premier testing standards to provide the technical expertise and make the product formulation more effective.
Raw Material Store
Raw materials require cool, dry conditions for storage. The stock room and methods of storage are designed to facilitate the observance of hygiene. The handling methods are naturally; of course, suit the type of building, situation of the stock room, and the quantity of raw materials being handled. The establishments are being able to cope with the intake and distribution of raw materials by the use of pallets and fork lift devices. These also assist in the rotation of stocks and in moving goods for cleaning under and behind. Goods are never being stored directly on the floor.
FIFO, First-In, First-Out FIFO rotation method ensures that our company is serving safe products and reducing spoilage.
Division of area or identification storage and labeling of raw and packing materials:
Green– For approved materials, Yellow– for Under test materials, and Red– for Rejected materials.
Identification area with colored plate will be displayed with material with the following details:
Item/Material
Date of Receipt
Supplier
Lot Number
Quantity
QC Number
Signature
Production
Pharmaceutical manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs as part of the pharmaceutical industry. Manufacturing in all sections is done under guidelines of Good Manufacturing Practice is a system to ensure that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
Tablet Section
A tablet is a pharmaceutical oral dosage form or solid unit dosage form. Tablets may be defined as the solid unit dosage form of medicament or medicaments with suitable excipients. It comprises a mixture of active substances and excipients, usually in powder form, pressed or compacted from a powder into a solid dose.
Liquid Section
These plants are quality tested on several parameters to assure its flawlessness. The offered plants are designed from the utmost grade raw material and innovative techniques in accordance with the set norms of quality.
Granules section
Granulation is a process of producing granules generally. In pharmaceutical manufacturing, granulation process implies the techniques that are, used to combine powdered particles to form relatively bigger ones called granules. This allows particles to stick together more firmly. It increases the particle size of the constituents used, which are mostly very fine powder. The greater is the particle size of the constituents, greater will be its compressive or binding ability.
Quality Assurance Section
Quality assurance (QA) is essential for ensuring that pharmaceutical products are manufactured to a safe and consistent standard. QA is a very broad field that refers to any aspect that may affect a drug’s quality during its research, development, manufacturing, and sales phases.
Quality Control Lab
Pharmaceutical quality control testing is usually a matter of repetitive testing of samples of APIs or of a limited number of pharmaceutical products. Quality control laboratory is able to deal with a much wider range of pharmaceutical substances and products and, therefore, apply a wider variety of test methods.
Quality control laboratory perform all quality control activities, e.g. sampling, testing of APIs, excipients, packaging materials and/ or pharmaceutical products, stability testing, testing against specifications and investigative testing.
The laboratory maintains a registry with receiving, distributing and supervising the consignment of the samples to the specific units and keeping records on all incoming samples and accompanying documents.
Each item of equipment, instrument or other device used for testing, verification and calibration should, when practicable, be uniquely identified.
Micro Biology Lab
Pharmaceutical plants must have controlled Environment with specific limits depending on the product it produce , also water used in Pharmaceutical industry must be purified.
Pharmaceutical plants have to follow guidance of GMP (good manufacturing practice).
Microbiology lab is the place where all microbiological tests and analysis occur, it have special preparations in design and precautions.
Packing Material Store
Approved packing material is placed in the respective places in the packing material stores. The packing material for primary packing will be kept in double wraps to prevent that from contamination. The approved material will be kept on the respective shelves as per the size and type of material without intermixing two batches of the same material.
FIFO, First-In, First-Out FIFO rotation method ensures that our company is serving safe products and reducing spoilage.
Division of area or identification storage and labeling of raw and packing materials:
Green– For approved materials, Yellow– for Under test materials, and Red– for Rejected materials.
Identification area with colored plate will be displayed with material with the following details:
Item/Material
Date of Receipt
Supplier
Lot Number
Quantity
QC Number
Signature
Finished Go down Store
After final packing products are stored in Finished Goods stores of warehouse and after Quality control and Quality Assurance released products are dispatched to market.
FIFO, First-In, First-Out FIFO rotation method ensures that our company is serving safe products and reducing spoilage.
Division of area or identification storage and labeling of raw and packing materials:
Green– For approved materials, Yellow– for Under test materials, and Red– for Rejected materials.
Identification area with colored plate will be displayed with material with the following details:
Item/Material
Date of Receipt
Supplier
Lot Number
Quantity
QC Number
Signature
Sales & Marketing Department
Pharmaceutical plants must have controlled Environment with specific limits depending on the product it produce , also water used in Pharmaceutical industry must be purified.
Pharmaceutical plants have to follow guidance of GMP (good manufacturing practice).
Microbiology lab is the place where all microbiological tests and analysis occur, it have special preparations in design and precautions.
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Kmpharma118@gmail.com
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Chak no. 118/10.R, Teh: Jahania, Dist: Khanewal
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0333-4021111
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