As a symbol of trust and high quality, Science Arts creates value for its customers. In 2002, it received its manufacturer’s licence for Chinese proprietary medicines from the Health Science Authority. Based on traditional medicinal formulas, and with the help of modern technology, it is able to develop new products and innovative techniques.
Science Arts abides by the Good Manufacturing Practice, also known as the GMP, for corporate skills upgrading. In 2007, it was awarded the GMP Certification by HSA, as it fulfilled all requirements stipulated by the authority. This achievement paved the way for the globalisation of Science Arts’ products.
A high standard clean room is a prerequisite of product quality assurance.
Science Arts is equipped with class 100,000 clean rooms that are certified by professional organizations. Equipments in the company possess high level of automation, satisfying GMP requirements.
Based on traditional medicinal formulas, and with the help of modern technology, it is able to develop new products and innovative techniques.
In accordance with GLP requirements, Science Arts has formulated standard operating procedures (SOP) for raw materials, intermediary and finished products, making use of high-performance liquid chromatography (HPLC) and atomic absorption spectroscopy (AAS) to establish a method for content and toxic heavy metal determination, that can be used to measure the content of various components according to control standards so as to ensure uniform and stable product quality.
Science Arts has implemented the following quality assurance management: supplier management, packaging materials printing management, material procurement and management, authentication management, production management, document control management, inspection management, measurement controls, training management, equipments management, product quality control management, adverse drug reaction report management, drug sales management, product release management and record control management, substandard drugs and other quality assurance system management, user feedback processing procedures and product recall management.