Anhui Cleanpro Biotechnology Co., Ltd., founded in 2015 and located in Tianchang City, Anhui Province, is a professional manufacturer of high-quality medical packaging. With extensive experience in the medical and pharmaceutical packaging industry, we are dedicated to delivering reliable products.

To meet the stringent cleanliness requirements of the pharmaceutical industry, we operate Class C+A clean workshops. All processes strictly adhere to GMP standards, encompassing facility design, environmental control, equipment validation, and personnel training.

Class C + A GMP production

Our main product is the Tyvek Ultraclean Steam Bag. We implement strict quality control from raw material procurement through production to finished products. Certified to ISO 15378, we strive to provide the highest quality products and services to our customers.

We continuously focus on R&D and innovation in sterile, dust-free technology. Furthermore, we are committed to building a professional technical team to earn the trust of global customers in our products and services.

Class C+ A clean workshops with all processes strictly adhering to GMP standards — facility design, environmental control, equipment validation and personnel training — for excellent microbial barrier and sterility assurance.

Controlled environment & monitoring

Two independent air purification systems — one dedicated to Class A environment control, one to environmental monitoring and inspection control — plus real-time monitoring and batch inspection throughout production.

Customization & validation support

Non-standard size customization supported across product lines; Beta Bag custom specifications take 2–4 weeks. Complete validation protocols and performance test reports assist process validation and GMP audits.

Selected customers

Roche, Pfizer, MSD, WuXi AppTec, BeiGene, Akeso, Qilu Pharmaceutical, Hualan Biological, Junshi Biosciences, CNBG, SPG and Luye Pharma. The Beta Bag has served multiple domestic ADC pharmaceutical companies.

Raw Material

Inspection

Cleanroom

Bag Making

Heat Sealing

In-line

Inspection

Fina

Sterilization

Packaging&Release

Quality Control Key Points

• Incoming Raw Material Inspection

• In-process Quality Monitoring

• Seal Strength & Integrity Testing

• Microbial Contamination Control

Entire process complies with GMP and ISO 15378 requirements, ensuring reliable and stable sterile packaging solutions.