Bioprocessing single-use systems
GMP CompliantUSP Class VIISO 13485:2016CE / FDA Registered

GMP Compliant Cell Culture Consumables & Biotech Consumable Solutions for Global Life Science & Pharmaceutical Industry

USP Class VI compliant lab consumables supplier, serving pharmaceutical enterprises, CDMOs & research institutes across 50+ countries

Quality Assurance

ISO 13485 & cGMP Quality Management System | Full batch traceability, endotoxin/nuclease strict testing

Global Delivery

Stable Global Logistics & Local Warehousing Support | DDP delivery for North America, Europe & Southeast Asia

Technical Support

24/7 Multilingual Technical Support | Application guidance for cell culture, lyophilization & biopharma upstream process

Custom Solutions

Custom Consumable Development | Custom surface treatment, packaging & specification for pharma pilot & production projects

Aseptek BioScience

About Aseptek BioScience

Founded in 2018 and headquartered in Zhangjiang Hi-Tech Park (Shanghai Biomedical Core Cluster), Aseptek BioScience specializes in the R&D, manufacturing and global sales of cGMP-compliant bioscience consumables, covering six core product lines: cell culture consumables, separation & purification filters, closed single-use fluid pathway systems, sterile isolator dedicated consumables, sterile injectable packaging materials and pharmaceutical QC testing auxiliary consumables.

Our quality system is fully certified to ISO 13485:2016 & CE standards, with core product lines completed FDA device registration. Our products are exported to more than 50 countries and regions, serving over 1000 global clients covering top pharmaceutical enterprises, CDMO facilities, academic research institutions and clinical hospitals.

50+
Countries & Regions
1000+
Global Clients
500+
SKU & Customized Solutions
8 Yrs
Biotech Consumable Experience
Learn More About Us

Why Choose Us

We integrate cGMP certified quality, biopharma-focused R&D, advanced cleanroom manufacturing and localized global service, to be your long-term reliable partner for bioprocess consumables.

Certified Quality

ISO 13485:2016 & CE certified, core product lines completed FDA device registration. Full lifecycle QC management from raw material incoming inspection to finished product release, complying with cGMP & USP material standards.

R&D Driven

In-house bioprocess R&D team focuses on customized consumable development for peptide CDMO, CGT and vaccine manufacturing, iterating products to match evolving biopharma process requirements.

Advanced Manufacturing

Class 100,000 Grade A/D cleanroom production workshops, automated production lines, SAL 10⁻⁶ validated sterilization process, stable batch consistency and low bioburden for biopharma aseptic production.

Global Service Network

Regional overseas warehouses across key global regions, localized English-speaking technical support team, fast after-sales & on-site technical service for clients in 50+ countries and regions.

Custom Solutions

Flexible OEM & ODM customization capabilities, supporting bespoke size, material, packaging & process validation documents, fully matching CDMO and pharmaceutical factory exclusive workflow demands.

Reliable Supply Chain

Dynamic inventory reservation system + mature cross-border DDP logistics, stable stock reserve for bulk & long-term recurring orders, guaranteed on-time delivery to US and EU production bases.

Bioprocessing single-use systems

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