

Parallel Single-Use Bioreactor System
平行一次性生物反应器系统
- SKU PAB-0004
- Parallel Bioreactors
- CE (to be confirmed)
- ISO 13485 manufacturing (to be confirmed)
- ISO 11137 sterilization (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Working volume | 0.1–10 L per bag |
|---|---|
| Bag count | 4–16 |
| Mixing | Stirred, rocking or shaken |
| Temperature range | 10–50 °C |
| Gas control | Independent air, O2, N2, CO2 |
| Sensors | Single-use pH and dissolved oxygen |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 9001, ISO 13485, 21 CFR Part 11
What is the Parallel Single-Use Bioreactor System?
A parallel single-use bioreactor system runs several disposable bags in one platform, avoiding cleaning between experiments. It suits multi-product development, clinical process work and studies that demand rapid turnaround and flexibility between conditions.
What is the Parallel Single-Use Bioreactor System?
A parallel single-use bioreactor system runs several disposable bags in one platform, avoiding cleaning between experiments. It suits multi-product development, clinical process work and studies that demand rapid turnaround and flexibility between conditions.
Overview
A parallel single-use bioreactor system places several pre-sterilized bags on a shared platform, each with its own mixing, gas supply and single-use sensors. Stirred, rocking or shaken bag formats can be used, and the platform coordinates temperature, feed and gas control across all bags with independent recipes. Because the fluid path is discarded after each run, no cleaning or cleaning validation is needed, and changeover between conditions is fast, which suits multi-product development and clinical process work. Volumes typically range from a fraction of a litre to a few litres per bag. Extractables and leachables data, bag integrity and single-use sensor performance must be managed, and the platform must confirm that each bag has independent control so that conditions do not interfere.
How does it work?
A parallel bioreactor system provides several small cultivation compartments, each with its own or multiplexed control of temperature, pH, dissolved oxygen, gas flow and feeding. Because each vessel follows a separate recipe, one experiment can compare many conditions under otherwise identical handling, which improves statistical power and reduces material and time per data point. Mixing and gas exchange are achieved by miniature impellers, shaking or gas-driven flow, depending on the format, and small volumes reduce medium, inoculum and reagent consumption. Shared software coordinates calibration, start and sampling and presents overlay plots for direct comparison. The main technical challenges are keeping control and hardware identical across vessels, avoiding cross-contamination and ensuring that results transfer to larger scale.
What are the key features?
- Multiple pre-sterilized bags on one platform
- Independent recipe and gas control per bag
- Stirred, rocking or shaken bag options
- No cleaning or cleaning validation between runs
- Single-use sensor integration
What are the technical specifications?
A typical parallel single-use bioreactor system configuration offers working volume of 0.1–10 L per bag, bag count of 4–16, mixing of Stirred, rocking or shaken, temperature range of 10–50 °C, gas control of Independent air, O2, N2, CO2 and sensors of Single-use pH and dissolved oxygen. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The Parallel Single-Use Bioreactor System is used in multi-product process development, clinical process characterization, scale-down modelling and cell and gene therapy development. Across the wider Parallel Bioreactors class, laboratories also deploy it for strain and clone screening, design of experiments studies and media and feed optimization.
Which standards and certifications apply?
Relevant standards and methods include ISO 9001, ISO 13485, 21 CFR Part 11, EU GMP Annex 11, ICH Q11, USP <87>, USP <88> and IEC 61010-1. Certification candidates for this model are CE, ISO 13485 manufacturing and ISO 11137 sterilization; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Standardize inoculation density, probe calibration and medium preparation across all vessels, because small differences become large when results are compared. Calibrate pH and dissolved oxygen probes as a batch and verify temperature uniformity before a comparative run. Keep the vessels and headplates clean and traceable to their positions to avoid cross-contamination. Record which recipe and vessel were used for each result, and keep a batch log linking conditions to outcomes. Because miniature sensors and small volumes can drift or evaporate, monitor evaporation and correct data accordingly. For regulated work, treat the system as measuring equipment with defined qualification and calibration intervals.
How do I select the right Parallel Single-Use Bioreactor System?
Choose a parallel single-use platform when changeover speed and multi-product flexibility matter. In an RFQ specify the bag volume and count, the mixing format, the control independence, the single-use sensor options, extractables documentation and the recording features.
How does it compare with other Parallel Bioreactors variants?
Choose the format from the number of conditions and the level of control required. Microbioreactor arrays suit early screening of many conditions with limited material, mini-bioreactors add real pH and dissolved oxygen control for deeper study, and bench-scale parallel vessels reproduce larger bioreactors closely for scale-down and process characterization. Confirm that each vessel has genuinely independent control, because shared gas or temperature systems can couple the experiments. Check working volume, agitation and aeration capability, the number of feed and sampling ports and whether automated sampling or dosing is available. Review the software for recipe management, overlay comparison, data export and, for regulated work, audit trails. Finally, confirm how results and parameters transfer to a single larger bioreactor.
Full specifications
| Working volume | 0.1–10 L per bag |
|---|---|
| Bag count | 4–16 |
| Mixing | Stirred, rocking or shaken |
| Temperature range | 10–50 °C |
| Gas control | Independent air, O2, N2, CO2 |
| Sensors | Single-use pH and dissolved oxygen |
| Sterilization | Gamma irradiation 25–40 kGy |
| Data output | Per-bag batch records |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Multi-product process development
- Clinical process characterization
- Scale-down modelling
- Cell and gene therapy development
Key features
- Multiple pre-sterilized bags on one platform
- Independent recipe and gas control per bag
- Stirred, rocking or shaken bag options
- No cleaning or cleaning validation between runs
- Single-use sensor integration
Frequently asked questions about Parallel Single-Use Bioreactor System
Each bag is new, so no cleaning runs between conditions and there is no carry-over risk. This shortens setup, allows rapid changeover between products and supports clinical work where cleanliness and traceability are essential.
Quality varies with film, sensor lot and calibration method, so laboratories verify sensors against offline measurements and keep lot records. Supplier quality agreements and change control help maintain consistency across a study.
Bag film strength, support design and mixing capability set practical limits, typically a few litres per bag in parallel formats. Larger volumes use dedicated single-use bioreactors or stainless vessels, where parallelism is limited but scale is greater.
It compares many strains, media or process conditions under otherwise identical handling, producing more data per experiment and per gram of material. Uses include clone screening, design of experiments studies, media optimization and scale-down modelling of production bioreactors.
The number follows the factors and replicates you need. A design of experiments with three or four variables typically needs eight to sixteen vessels, while simple screening may need four. More vessels usually mean smaller working volumes to keep the platform manageable.
They are comparable if inoculation, calibration and mixing are consistent across vessels and each has independent control. Shared gas, temperature or feed systems can couple the vessels, so verification of independence and consistent handling is part of using the platform correctly.
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