Asia Stem Cell Center

About Us

Asia Stem Cell Center (ASC) is a stem cell processing laboratory that has an operational permit certificate from the Indonesian Ministry of Health where stem cell processing and processing uses Good Manufacturing Practice (GMP) standards.

The products produced are stem cells, stem cell metabolites for degenerative diseases, immune diseases and cancer.

stem cell

Stem cell, cell and metabolite products are tailor made according to the disease state and patient status

ASC laboratories collaborate with both the teaching hospital and regular hospital

Good Manufacturing Practice guidelines set out quality control standards for the manufacturing of medicinal products. They aim to ensure that pharmaceuticals such as pills or vaccines have consistent strength, purity and quality. GMP guidelines cover quality assurance measures for all aspects of manufacturing – from premises, equipment and staff training, to operational processes, packaging and storage conditions – as well as overarching quality assurance and documentation systems. 

GMP address the requirements for the air of a clean room, whereas other parts target all materials and reagents used in the production of a particular drug. It also specifies how far a manufacturer must be able to trace back the source of each ingredient in the final product and, of course, how final testing of the product is performed before release.

Sources

GMP STANDARIZED LABORATORY