Close-up laboratory flasks with pharmacy medicine drag in cartridge. Shallow DOF

Our associated contract manufacturing facilities are built according to International regulatory guidelines and are approved by recognised regulatory authorities like EU-GMP, USFDA, TGA Australia. Our associated contract manufacturing facilities have capability to manufacture tables, capsules, oral liquids, creams, ointments, sprays, sterile parenteral and ophthalmic preparations.

The quality management systems followed in the manufacturing facilities ensures ongoing compliance with good manufacturing, good laboratory, and good documentation processes throughout the product life cycle. 

We adopt Quality by Design concept and ensure the quality, safety and efficacy of our products are met through continuous improvements. Our purpose is to bring cures to patients with the quality medicines that we manufacture. We see our families as an end user of our medicines.

TGA is an Australia’s government authority responsible for evaluating, assessing, and monitoring products that are defined as therapeutic goods. TGA regulates medicines, medical devices, and biologicals to help Australians stay healthy and safe. Seed Pharma follows the regulations and provides the services per TGA.