In accordance with Faizyme’s commitment to the achievement and maintenance of the highest possible Quality Systems and Practices throughout all avenues of the Company’s Operation, Faizyme set the objective of actively implementing the required standards of documentation and quality practices defined by the International Organisation for Standardisation (ISO). In March 1997, Faizyme’s Quality Systems were certified to conform to the requirements of ISO 9002.
Faizyme’s Quality Management System is now certified to conform to the standards of ISO 9001. In addition, Faizyme’s facilities and manufacturing processes are certified to meet the requirements of Good Manufacturing Practices (GMP) in accordance with the World Health Organisation (WHO) guidelines for pharmaceutical/biological products.
On-going training is given to all staff in the elements of the ISO programme and the various internal procedures that have been documented at Faizyme. Internal audits of all aspects of the company are performed in accordance with a defined audit program and Management Reviews of the Company’s Quality System are conducted.
All products prepared are fully tested to assure conformance with specifications and a Certificate of Analysis is issued and accompanies each batch of product supplied to customers. We appreciate receiving any comments or suggestions from our customers on any aspects of product quality since this will assist us in our quality improvement programme and thereby enable us to ensure that the needs of our valued customers are met.
For certificates refer to downloads.