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Quality Policy
Quality Management
Quality Systems
Laboratories
The Manufacturing Facilities
Storage Facilities
Key Personnel
Health & Hygiene
Utilities
Air Handling And Ventilation Systems
Documentation & Validations


QUALITY POLICY
ASIA's QUALITY POLICY aims at research , development , manufacturing and marketing of safe , effective and affordable quality medicines meeting the international specifications , to satisfy the customer needs and to help people live a better quality of life. It is always ASIA's endeavor to provide assurance and safety of medicines to meet the customer's expectations by offering consistent quality products through cGMP.and leadership.


QUALITY MANAGEMENT

At ASIA we believe that Quality Assurance , current Good Manufacturing Practices and Quality Control are inter related. Good Laboratory Practices and Good Storage Practices are in place.
- Products are designed and developed in a way to inbuilt quality into them.
- Adequate facilities, trained personnel and approved procedures are available for sampling, inspection and testing of materials at all stages.
- Regular monitoring and stability testing is done on a continuous basis to ensure shelf life of the products.
- Arrangements are made so as the products are stored, distributed and handled to ensure quality throughout the shelf life.


QUALITY SYSTEMS

Quality Systems at ASIA are supported by
- Well trained personnel
- Well planned construction
- Proper machineries and continuous maintenance
- Sourcing raw materials to meet to international standards
- Well equipped laboratories to follow Good Laboratory Practices
- Separate stores for raw materials and finished products to follow Good Storage Practices
- Proper operating instructions and manuals
- Follow-up of documents throughout all stages of production to ensure safe operation and control.

LABORATORIES
ASIA is well equipped with the following laboratories to meet the requirements.
- Research and Development Laboratory
- Chemical Laboratories
- In process Control Laboratories
- Biological Laboratories

THE MANUFACTURING FACILITIES
To cater to the needs of the organization, the Board of Directors have always taken interest to select the most qualified manpower including pharmacists, chemists and technicians. The Board of Directors have always been ensured to procure raw materials from trusted brands from all over the world.

The manufacturing plant of ASIA is situated at a pleasant location, in the outskirts of ALEPPO city. The year 1998 was a turning point in the history of the company with the introduction of facilities for sterile formulations. The total area of the site is over 100,000 sq. mts and the total build up area is about 60,000 sq. mts. And the plant consists of the following departments.

- Tablets department ( plain and coated )
- Oral Hormones department
- Oral Penicillins department ( Dry Syrups , Capsules and Tablets )
- Oral Cephalosporins department ( Dry Syrups , Capsules and Tablets )
- Oral Liquids department
- Semisolids Department ( Ointments , Creams , Gels and Suppositories )
- Powder Injectable Vials for Penicillins plant
- Powder Injectable Vials for Cephalosporins plant
- Liquid Injectable Vials and Ampoules for non Hormones department
- Liquid Injectable Vials for Eye Drops section
- Liquid Injectable Vials and Ampoules for Hormones department
- Herbal Medicines and Plant based products department
- Soft Gelatins department

A broad range of products representing a cross section of formulations and therapeutic categories are produced at ASIA. The products currently produced are about 200 in number and there are about 50 products at different stages of development / registration for approval.
ASIA produces different products under the license of some foreign companies. Some of them are:
Jena Pharma (Germany); Slovako Pharma (Slovakia) ; Dentinox (Germany) ; Vega (England)
Jedeon Richter (Hungary); Danish Pharma (Denmark) ; Mebaco (Egypt) ; IBI (Italy)

STORAGE FACILITIES
Raw materials , semi finished products , finished products and packaging materials are stored as per the requirements in the respective areas , needing conditions like temperature , humidity etc.

KEY PERSONNEL
At ASIA , key persons are identified and all the critical operations are controlled and supervised by the key persons who are experienced and qualified for the same.

TRAINING
To upgrade the skills of the plant personnel with a view to achieve better standards, Training of all the personnel in the areas of Production , Quality Control , Engineering and Plant Administration is carried out in the following areas.
- Current Good Manufacturing Practices, W.H.O Regulations
- Technical training
- Standard Operating Procedures

HEALTH & HYGIENE
Employees who are healthy and are free from any contagious or infectious diseases are only engaged in Production, Quality Control Engineering and other related areas. Personnel hygiene and sanitation are well maintained.

UTILITIES
At ASIA we produce our own Steam, Purified Water, Oil Free Compressed Air, Nitrogen and Vacuum centrally.
The DG sets provide the back up in case of power failure.
Pure Steam and Water for Injection are produced in the respective blocks as per the requirement.

AIR HANDLING AND VENTILATION SYSTEMS
- Manufacturing areas in different independent blocks are supplied with Temperature controlled clean air. A number of Air Handling Units and Ventilation Systems are installed to serve the purpose.
- Air Handling Units are dedicated in case of areas where it is required . HEPA filters are installed in all the Critical Areas and areas supporting the Critical Areas.
- Humidity is controlled and maintained in areas where the Product / Operation requires low humidity conditions.
- Positive Pressure Gradients are maintained on a continuous basis in all the Critical Areas. Records are maintained.

DOCUMENTATION & VALIDATIONS
- At ASIA , to comply with the Good Manufacturing Practices, an elaborate Documentation System has been implemented.
- All the requirements of Processing, In-Process checks, Testing, Release etc. were documented in the form of various specifications. Nothing is left to chance. to avoid errors and inconsistent performance.
- Periodic Validations of all the Critical Operations , Environment and the Machines are carried out by a team of representatives from Quality Assurance , Production , Engineering and if necessary an out side consultant

 

 

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