top of page
Pharmaceutical/
Biomedical/
Medical
Pharmaceutical/Biomedical/Medical Industry
The production and economic survival of pharmaceutical/biopharmaceutical/medical device manufacturers largely depend on the safety of the finished product. Therefore, it is necessary to know the potential sources of pollution, and pollution control sources require clean rooms.
A major design aspect of a cleanroom is to extract each manufacturing process, identify key work steps, and classify the corresponding cleanroom categories for manufacturing.
For pharmaceutical/biopharmaceutical/medical device production cleanrooms, it usually ranges from ISO 5 to ISO 7. Through the experience of our professional team, we will provide comprehensive cleanroom solutions.
![ISO](https://static.wixstatic.com/media/8b581e_4b3d86570eba4082a59cecd1577abd7e~mv2.png/v1/fill/w_49,h_22,al_c,q_85,usm_0.66_1.00_0.01,blur_2,enc_auto/8b581e_4b3d86570eba4082a59cecd1577abd7e~mv2.png)
ISO
![Pharm_Bio](https://static.wixstatic.com/media/8b581e_2cc0b07f06d74814b517e2aa00759c41~mv2_d_4256_2832_s_4_2.jpeg/v1/fill/w_147,h_98,al_c,q_80,usm_0.66_1.00_0.01,blur_2,enc_auto/8b581e_2cc0b07f06d74814b517e2aa00759c41~mv2_d_4256_2832_s_4_2.jpeg)
Pharm_Bio
![ISO](https://static.wixstatic.com/media/8b581e_4b3d86570eba4082a59cecd1577abd7e~mv2.png/v1/fill/w_49,h_22,al_c,q_85,usm_0.66_1.00_0.01,blur_2,enc_auto/8b581e_4b3d86570eba4082a59cecd1577abd7e~mv2.png)
ISO
1/2
bottom of page