The construction of GMP biopharmaceutical factories must create qualified layouts and reasonable production sites to ensure that drug production meets the requirements of ensuring quality. The production process of biopharmaceuticals is becoming increasingly complex, with a wide variety of raw material specifications used, which can easily cause human errors and cross contamination of products. To prevent mixing and cross contamination between people and logistics, the standardized design of clean rooms is extremely important. Through in-depth research on the production environment of biopharmaceutical customers and accumulated engineering experience, Shenzhen Jinyunding Engineering Co., Ltd. has a clear understanding of the key to environmental control in the biopharmaceutical production process. Energy saving systems are also of utmost importance in providing solutions, in compliance with GMP and ISO14644, IEST, EN1822 international standards, and applying innovative green and energy-saving process technologies to environmental solutions.