GMP Guiding Principle: ICH Q7
ISO 9001:2008 Certificated

We focus on quality, and to standardize the management, technology and strict quality control and verification system to ensure the safety of production processes, high efficiency, high stability,
each batch of products can achieve reliable and stable quality.
Our quality assurance (QA) team ensures that every stage of the manufacturing process (receiving of raw materials, release of intermediates and active pharmaceutical ingredients, testing and packaging) meets all customer and regulatory expectations, whether the product is going into the US or European markets.
Our QA team works closely with clients to facilitate site audits and manages any quality issue that may arise during the manufacturing.

Document control
Batch record review
Product release
Qualification & validation activities
Change control compliance
Supplier qualification and audits