MFG. Facility

MANUFACTURING_FACILITY

Pharmaceutical manufacturing facilities play a crucial role in the production and distribution of life-saving drugs and medications. These facilities are designed to meet strict regulations and standards set by regulatory agencies such as the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA).

The primary objective of a pharmaceutical manufacturing facility is to produce high-quality and safe drugs for patients. To achieve this, the facility must have a well-designed infrastructure that is equipped with state-of-the-art technology, equipment, and processes. The manufacturing process begins with the receipt of raw materials and ends with the final packaging and distribution of the finished product.

A typical pharmaceutical manufacturing facility includes several key departments such as quality control, research and development, production, and packaging. The quality control department is responsible for ensuring that the raw materials, intermediate products, and finished products meet the required standards. This department performs a series of tests and checks to ensure the quality and safety of the products.

The research and development department is responsible for developing new drugs and improving existing ones. This department works closely with the quality control department to ensure that the drugs meet the required standards and are safe for human consumption.

The production department is the heart of the pharmaceutical manufacturing facility. This department is responsible for the  drugs. The production process involves several steps such as blending, granulation, compression, and coating. The equipments used in the production department are designed to meet the highest standards of quality and safety.

The packaging department is responsible for packaging the finished products and preparing them for distribution. This department uses sophisticated equipment to ensure that the products are packaged properly and are ready for shipment.

We have WHO-GMP Certified Unit. To ensure the quality and safety of the drugs, pharmaceutical manufacturing facilities must follow strict regulations and standards set by regulatory agencies such as the FDA and EMA. These regulations cover all aspects of the manufacturing process, from the receipt of raw materials to the final packaging and distribution of the finished product.

In conclusion, pharmaceutical manufacturing facilities play a crucial role in the production and distribution of life-saving drugs and medications. These facilities must meet strict regulations and standards set by regulatory agencies and must have a well-designed infrastructure that is equipped with state-of-the-art technology, equipment, and processes. The primary objective of a pharmaceutical manufacturing facility is to produce high-quality and safe drugs for patients.

Highlights of Our Manufacturing Facility :

  1. The complex also houses its own R &D facility for in-house product development.
  2. Air environment conditioned in each area with respect to temperature, humidity, filtration, particle counts, etc.
  3. No wood or asbestos component.
  4. Accessibility of all utilities and maintenance areas from outside, for additional ease of operation.
  5. Each zone has separate AHUs (Air Handling Units), dehumidification units, and dust extraction systems.
  6. Segregation of every critical processing activity in each zone, to avoid cross-contamination.
  7. Ample segregated storage for raw materials and packaging materials, with a quarantine facility.
  8. Individual compression and coating cabins with separate air handling units to avoid cross-contamination.
  9. Duo Pass Reverse Osmosis (RO) water system/ de-mineralization plant.
  10. Zero-discharge Effluent Treatment Plant.
  11. Air-conditioned stores for raw materials, packing materials, and finished goods.
  12. Isolated and dedicated production facilities for β-Lactum and Cephalosporin dosage forms.
  13. Dispensing of materials under an SS reverse laminar flow.
  14. An alternative power generation system for uninterrupted production.
  15. A unidirectional flow of men and materials to promote optimum productivity
  16. We house huge capacities for manufacturing round the clock (* Spare capacity available for all sections).
  17. Respective zones, areas, and even uniforms marked with specific colors to ensure total segregation.
  18. Separate air handling units for every production department, in addition to air conditioning with 3-micron filtration, to ensure absolute product purity.

We meet the most demanding customer specifications while offering the most aggressive pricing in the industry. In addition, we offer our products through third parties and have private label agreements for export. We manufacture different brands of pharmaceutical formulations in different forms. We look forward to working with importers, distributors, and agents to increase our market share.