The "modular" concept in AksobioQ refers to deconstructing the cleanroom into prefabricated, combinable units with independent functionality. Each module integrates piping, HVAC, electrical, and intelligent systems in the factory, forming "plug-and-play" functional packages. On-site assembly is as simple as stacking building blocks, enabling rapid construction of customized clean spaces. This approach shortens facility build times by approximately 90%, minimizes on-site construction disruptions, allows flexible layout of functional units, and supports non-disruptive expansions via horizontal or vertical configurations-ensuring zero production downtime. Leveraging IoT for real-time monitoring enhances operational reliability, achieving an optimal balance of efficiency and cost.

The mobility of container structures provides AksobioQ with numerous advantages. The robust shell and standardized dimensions ensure exceptional transportability, compatible with global logistics networks. In the event of relocation, the containerized cleanroom can be fully transported and rapid deployed, avoiding the substantial capital and resource waste associated with dismantling traditional cleanrooms. Furthermore, the container design facilitates asset recovery and reuse; mismatched modules can be traded, recycled by our company, or replaced during production line adjustments or process upgrades, yielding significant cost savings.

As a containerized modular cleanroom, AksobioQ offers distinct advantages over traditional cleanrooms: standardized manufacturing, mobility, ease of replacement, rapid deployment, streamlined processes, reduced on-site installation risks, immediate usability, and phased investment options.

Compared to similar modular cleanrooms, AksobioQ stands out with Medointec's 30 years of industry expertise, providing one-stop turnkey services. Manufactured in China with the world's most robust supply chain, it ensures reliability and cost-effectiveness.

Yes, AksobioQ is suitable for direct outdoor deployment. Its durable containerized exterior maintains stable operations in external environments.

When process workflows evolve, AksobioQ's spatial configuration can be restructured accordingly. By reorganizing or replacing modular units, it allows flexible adjustments to space size, functional zoning, and system layouts. AksobioQ also delivers high flexibility and sustainability. For relocations, it supports complete transport to new sites and reactivation, eliminating the resource waste of traditional cleanroom demolition and rebuilds.

The AksobioQ modular cleanroom excels in flexibility and adaptability, enabling reconfiguration for future production needs. In a rapidly changing market, your output may double in two years. AksobioQ facilitates easy disassembly, relocation, expansion, transfer, or reconfiguration.

AksobioQ's modular design allows enterprises to dynamically scale and direct fixed asset investments based on development plans and real-time needs, optimizing resource allocation. Companies can phase investments according to funding and growth pace-starting with core modules and incrementally adding or upgrading as business expands. This avoids the high sunk costs and waste inherent in traditional one-time large-scale builds.

AksobioQ is designed and manufactured at Medointec's facilities with full consideration of the target country's or region's regulatory standards, then shipped as fully assembled units for on-site installation. This mitigates risks from overseas permitting, team assembly, labor management uncertainties, extended construction delays, and budget overruns. It dramatically shortens international facility deployment times while reducing uncertainties from local regulations and market variances.

In the 3.0 shared economy era, AksobioQ's modular design and superior flexibility foster an innovative sharing model in biopharmaceutical R&D. Its core strength lies in recyclable, integrated industrial fit-out services, making it an ideal tool for biopharma parks to deliver differentiated value-added services.

AksobioQ enhances industrial park tenant attraction: Its adaptability allows parks to swiftly customize or adjust industrial spaces per tenant needs, providing "turnkey ready" conditions in minimal time and accelerating clean facility setup to draw premium biopharma enterprises.

AksobioQ reduces park operational costs: Its reusable nature eliminates repetitive large-scale fit-outs for each tenant.

Additionally, AksobioQ responds efficiently to changes: With rapid advancements in pharma regulations and markets, its modular setup enables quick adaptations to evolving layouts, compliance, and iterations.

AksobioQ offers diverse cleanroom solutions, including standardized and customized options to meet varied enterprise requirements.

Standardized products are designed around common industry processes; select modules based on your site and workflow. For complex processes beyond standard offerings, AksobioQ provides tailored customization.

To maximize space utilization in China, we recommend unit module dimensions of: Length: 9m, Width: 3m, Height: 3.4m.

Standard AksobioQ is primarily indicated for:

Cell culture rooms in universities, research institutes, and R&D labs: ：Click to download for more details

Somatic cell R&D, production, and QC：Click to download for more details

Virus R&D and production：Click to download for more details

Plasmid R&D and production：Click to download for more details

GMP microbial testing for pharmaceuticals：Click to download for more details

Standard single modules include: Modular enclosure structure, inter-module connection mechanisms, purification HVAC and piping systems, PLC control systems, interlock controls, lighting and UV sterilization systems, self-cleaning pass-through windows, exhaust and piping systems, constant temperature/humidity controls, variable air volume pressure regulation, drainage systems, gas supply systems, water supply systems, power distribution systems, on-site displays, etc. Other process equipment can be client-specified, self-provided, or procured on behalf.

AksobioQ's core clean zone achieves up to China 2010 GMP B+A cleanliness levels, adjustable per client needs. It complies with GB 50457 (Pharmaceutical Clean Plant Design Code), GB/T 25915.1-2021 (Cleanrooms and Associated Controlled Environments - Air Cleanliness Classification), ISO 14644, FDA, EMA GMP international standards, and domestic GMP regulations.

Opt for custom AksobioQ when needs exceed standard universality and flexibility is paramount. Recommended scenarios include:

1. When standard functions fall short of production processes

2. Site dimensions mismatch standards

3. Future functional adjustments or area expansions planned

4. Multifunctional integration required

5. Adaptation to special environments or climates

6. Compatibility with existing facilities

7. Unique or temporary projects

Medointec begins with on-site surveys and in-depth consultations to clarify process needs, incorporating your User Requirements Specification (URS). Balancing workflow and site constraints, we design a turnkey solution maximizing utilization. Upon approval, factory production yields a precisely matched product, shipped for installation. Click to download URS template.

It features data processing and real-time visualization for timely insights; integrates 3D visualization for intuitive spatial and environmental overviews; seamlessly interfaces with diverse lab equipment and systems. Employing enterprise-grade data acquisition ensures stability and reliability; supports heterogeneous database storage for varied needs; provides graphical displays of real-time/historical data with multidimensional trend analysis for informed decisions. Includes multilevel alarm services for prompt anomaly responses; enables easy data export for in-depth analysis and reporting. download

The system monitors/controls key parameters:

• Temperature (traceable)

• Relative humidity (traceable)

• Differential pressure (traceable)

AksobioQ cleanrooms incorporate monitoring compliant with ISO 14644 and GB 50457, capturing, recording, and alerting on parameters like temperature, humidity, gas concentrations, pressure, differential pressure, airflow, and equipment status for real-time analysis.

RDtoRA ensures data integrity via role-based access and comprehensive audit trails, maintaining authentic, reliable records. It monitors environmental parameters in real-time to uphold cleanliness standards. Granular permissions and approval workflows enhance security and compliance, supporting efficient lab operations and data protection.

Yes. RDtoRA can generate individual experiment reports or aggregate multiple into comprehensive summaries.

Yes, we configure customized solutions based on your needs.

Full Prefabrication Workflow: All functional modules (walls, HVAC, electrical, monitoring systems, etc.) are customized, assembled, and pre-validated in the factory. On-site, modular splicing enables immediate use.

Confirm AksobioQ dimensions, core clean zone grades and quantities, area layouts across zones, built-in equipment models, smart management system inclusion, enclosure material specs, clean air supply via HEPA/ULPA filters, positive/negative pressure, temperature/humidity controls, and specialized lighting.

Medointec conducts comprehensive testing post-installation and provides specialized training for your team to ensure seamless operation. We offer remote web-based maintenance (with network permissions), troubleshooting, on-site support, and ongoing training to optimize performance and maintain best practices.

AksobioQ provides factory pre-validation services: Medointec generates full cGMP documentation sets, enabling clients to demonstrate to regulators that facilities/equipment meet design intents and URS. This includes commissioning plans, FAT/SAT protocols (service purchase required), and pre-delivery DQ, IQ, OQ validation reports (service purchase required).

Medointec designs AksobioQ's tolerances based on site-specific conditions. Please consult our technical team for details.  (Contact Us)

Indoor deployment requires minimal foundational support: We provide professional pre-assessment guides and customized adaptations, evaluating floor flatness, utilities (water/electricity/exhaust/power), to ensure one-step installation.

Prior to installation, clear the area and relocate any equipment. Remove or elevate obstructing pipes, conduits,or sprinklers. Repair and level concrete slabs, installing vapor barriers as needed.

Outdoor deployment needs basic foundational support: Our pre-assessment guides and adaptations evaluate drainage, air quality, and dust/particulate levels for seamless installation.

AksobioQ is engineered to rigorous standards, including current Good Manufacturing Practices (cGMP), ISO classifications, U.S. FDA guidelines, EU EMA GMP, and client-specific regulations. Each prefabricated cleanroom includes a complete engineering handover package for full traceability and compliance assurance.

AksobioQ ensures seamless global localization. Whether destined for the Americas, Europe, or Asia-Pacific, we guarantee compliance with international certifications, dynamic alignment to target GMP/ISO norms, pre-configured power, units, and interfaces. Our experts address regulatory variances and provide customized submission support (service purchase required). For risk-free delivery, specify the target during surveys to initiate tailored adaptations.

AksobioQ manufacturing and installation timelines are markedly faster than traditional cleanrooms. Depending on scope and site readiness, standardized modules typically complete production and commissioning within 60 working days post-contract.