Actigen was established in 2017 with the goal of creating pharmaceutical and healthcare products with the highest caliber to satisfy both domestic and international markets with all major standard compliances such as Good manufacturing practice ,ISO standards etc. Since the initiation of this project, Actigen’s facilities and Utilities has been designed and constructed under supervision of professional team to rest assure that all specific requirements will be complied including tight adherence to Good Manufacturing Practice (GMP) guidelines. This guarantees that every product that leaves Actigen is the best possible and safe.
Every production step is strictly controlled within the Clean Room to ensure that each product is free from contamination, from manufacturing to packaging and storage
The laboratory is equipped with advanced tools and equipment for precise testing and analysis. The expert team conducts thorough inspections of raw materials, production processes, and finished products to ensure quality
The research team has expertise in various fields such as chemistry, biology, pharmacology, and biotechnology, driving innovation and pharmaceutical development
Modern and standardized storage system in a controlled temperature environment to maintain the effectiveness and safety of products and raw materials
Promote the use of renewable energy for electricity generation to reduce energy consumption and lower greenhouse gas emissions
Holding GMP Audit Facility license and GMP Audit license for pharmaceutical research
55/58 Village No. 3, Rama 2 Road, Na Di Subdistrict, Mueang Samut Sakhon District Samut Sakhon Province 74000
E-mail : [email protected]
