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WHO - GMP

WHO - GMP

Good Manufacturing Practice (GMP) is a system for ensuring 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. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff.

Detailed, written procedures are essential for each process that could affect the quality of the finished product. WHO (World Heath Organisation) has established detailed guidelines for good manufacturing practice. Many countries have formulated their own requirements for GMP based on WHO - GMP while others have harmonized their requirements, for example in the Association of South-East Asian Nations (ASEAN), in the European Union and through the Pharmaceutical Inspection Convention.

Unique lab Ltd. Has obtained WHO – GMP certificate for the manufacturing process in late 2010. The certificate was issued for the period of five years. After obtaining the WHO – GMP, Unique lab has gradually obtained Certificate(s) of Pharmaceutical Product(s) for all of its currently marketed products. This indicates that all Unique lab products are produced following all the guidelines and specifications as required by WHO good manufacturing practices.

About Us

 

 

 

About Us

Unique Lab  Ltd. was established in 2010 as a limited liability company.

The company was incorporated with the sole purpose of manufacturing and sale of affordable yet high quality generic pharmaceutical products. Our main goal is to provide an alternative for expensive drugs on markets of developing countries that cannot afford the expensive proprietary drugs.

The mission of Asia Pharma Ltd. is to improve the efficiency of healthcare systems worldwide by providing them more drugs of the same quality for the same money.

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