What is Black Biotechnology? 7 key security fields

What is black biotechnology? Definitions, applications and challenges

Black biotechnology is the branch of biotech focused on dangerous pathogens and their use for malicious or defensive purposes. It studies lethal microorganisms to neutralize them, but it also encompasses the possibility of designing biological weapons that are relatively easy to deploy. Put simply, it is a field “concerned with everything related to bioterrorism and biological warfare.” This includes researching drug-resistant germs (such as Bacillus anthracis, the cause of anthrax) to counter their harmful effects, while also acknowledging that the same know-how could be applied to build high-impact bio-weapons.

In short, black biotechnology investigates living organisms (viruses, bacteria, toxins) with two aims. On one hand, to develop countermeasures (vaccines, diagnostics, genetic defenses). On the other, to understand how these pathogens could be used in biological warfare and bioterrorism. Although most people associate biotechnology with health or agriculture, black biotechnology operates in the realm of national and global security, trying to stay ahead of emerging biological threats.

Current applications and examples of black biotechnology

Black biotechnology shows up in very specific projects and technologies. Highlights include:

  • High-containment labs (BSL-3/4). Governments and companies have built specialized facilities to study the most dangerous pathogens. For example, GSK opened in Tres Cantos (Madrid) what it described as the first BSL-4 lab owned by a pharmaceutical company, investing 4.5 million euros. In these labs, agents such as Ebola or Nipah viruses are handled, which can cause fatal disease in the absence of vaccines. There are roughly 51 BSL-4 labs in about 27 countries, double the number a decade ago. Europe has the most (25), followed by North America (14) and Asia (13). Another 18 BSL-4 facilities are slated to open in the coming years, especially in Asia (India, the Philippines, etc.). Along with “BSL-3 plus” sites, these facilities are essential to investigate dangerous germs without risk of environmental release.
  • Genomic surveillance and global networks. Worldwide systems are being developed to detect unusual outbreaks earlier. The WHO created the Berlin-based Pandemic Hub, which uses AI to analyze real-time data. Its EIOS platform aggregates public-health sources across the internet to flag emerging threats quickly. Pathogen genomics is also being scaled up: the International Pathogen Surveillance Network (IPSN) connects more than 235 organizations to sequence viruses and track variants. In Spain, the RE-LAB network coordinated by the ISCIII is tasked with early identification of suspicious samples. Technologies such as high-throughput sequencing (NGS) and bioinformatics enable rapid processing of large genomic datasets, speeding up the detection of new germs. In short, international surveillance brings together hospitals, specialized labs and digital tools to anticipate a pandemic before it explodes.
  • Genetic diagnostics and countermeasures. Black biotechnology uses gene editing as a defensive tool. CRISPR has been adapted to locate pathogens in minutes. Methods like SHERLOCK, DETECTR or CARMEN detect viral genomes (for instance, SARS-CoV-2) quickly and cheaply, potentially even in field settings. Beyond diagnosis, researchers are exploring CRISPR to inactivate viruses, for example by designing “molecular scissors” that cut viral RNA to block infection. Work is also advancing on therapies using modified viral vectors to detect and eliminate infected cells. In the future, disease vectors (like mosquitoes) could be genetically edited so they cannot transmit malaria or dengue, a preventative biodefense strategy. Together, these techniques enable faster vaccine development (mRNA vaccines) and novel therapies against biological agents.
  • Outbreak simulations and training. To prepare for attacks or pandemics, computational models and drills are used. The WHO’s Berlin hub is developing a pandemic simulator to model disease spread and test the impact of various health measures. Once in operation, it will give policymakers practical “what if” insights about quarantines or antivirals. Military and civilian response drills are also common, including exercises with chemical or biological agents to train epidemiologists and health systems. These simulations help assess the effectiveness of countermeasures before a real outbreak occurs.
Infographic showing black biotechnology applications including pathogen research, genetic defense, global monitoring, and biosecurity ethics

Black biotechnology, bioterrorism and biosecurity

Black biotechnology is tightly linked to deliberate threats. Bioterrorism is the criminal use of bacteria, viruses or toxins to cause illness, death and panic. Biological weapons are living agents engineered to trigger epidemics. In biological warfare, pathogens are used at scale for military ends, with the aim of terrorizing or weakening entire populations. Historical examples include throwing infected corpses to spread plague during the Middle Ages and multiple nations researching anthrax, cholera and other germs as weapons during World War II.

Black biotechnology feeds both the threat and the defense. On one side, it can reveal ways to create synthetic organisms with greater virulence. On the other, it generates countermeasures. A country committed to biodefense seeks to protect its population against intentional attack. In this context, it helps to distinguish biosecurity (protection against natural or accidental threats) from biodefense (protection against deliberate attacks). For instance, China has recently included “biodefense” in its national security strategy. Authorities around the world now stress stronger epidemiological surveillance to determine whether an outbreak is intentional or natural, while accelerating vaccine development against high-risk pathogens.

Research in this area carries risks. Since many scientific advances are dual-use, there is constant concern that measures meant to defend us (for example, open genomic databases or transparent research) could be exploited by malicious actors. Most countries lack specific regulation for dual-use research, meaning legitimate scientific work that could be repurposed as a weapon. Only Canada has legislation that broadly covers such experiments. Internationally, the Biological Weapons Convention (BWC), signed by 143 countries, lacks robust verification mechanisms, and powers such as China, North Korea or Israel have never ratified it. This creates an ethical and political dilemma. How do we advance defensive science without fueling a biological arms race.

Socially, black biotechnology triggers distrust and conspiracy theories, such as claims about COVID-19’s lab origin. The opacity of some high-risk labs heightens public fear. Experts therefore call for more transparency and shared biosafety standards, for example ISO-type norms for biosecurity management and ethics committees to review work with dangerous pathogens. Ultimately the ethical and political challenge is to balance security (not stifling useful science) with precaution (avoiding leaks and biocrime).

How it differs from other types of biotechnologies

Biotechnology is often color-coded by application. Red biotechnology focuses on health, including vaccines, gene therapies and recombinant medicines. Green biotechnology targets agriculture (GM crops, biofertilizers). White biotechnology centres on sustainable industrial processes (biofuels, biorefineries). There is also grey biotechnology (environmental bioremediation), blue biotechnology (marine biotech) and even gold biotechnology in some contexts.

Black biotechnology stands apart because it addresses security challenges. While the others seek direct benefits (health, food, clean energy), black biotechnology focuses on hostile pathogens and how to protect against them. In short, it investigates germs that could be manipulated for military ends. That is what makes it unique. Its goal is not to treat the general public, but to anticipate and neutralize threats. As a scientific discipline, it shares tools with the rest (genomics, genetic engineering), but it differs in its ultimate purpose.

Infographic on the different types of biotechnology

Leaders and countries involved

Countries investing most heavily in black biotechnology tend to have advanced public-health and defense programs. Europe hosts many BSL-4 labs, the UK, France, Germany, Sweden, Switzerland and others. North America also stands out, especially the United States, with numerous public and military high-containment facilities. In Asia, China and India have expanded their capabilities. Wuhan’s Institute of Virology is the world’s largest BSL-4, and the United States is bringing online the National Bio and Agro-Defense Facility at Kansas State University, with roughly 4,000 m² of lab space. Dozens of BSL-4 facilities were added in the US and Europe after 2001 to bolster biodefense.

According to the Global BioLabs report (NTU Singapore), there are 51 level-4 labs across 27 countries, three quarters of them in urban areas, which raises accident risk. In Latin America, Brazil and Mexico have reinforced epidemiological surveillance networks, for instance influenza and COVID labs. Biotech companies also participate. GSK’s Tres Cantos center in Spain leads anti-infective research and recently inaugurated its private BSL-4 site. 

Institutions like the Institut Pasteur, Kansas State University or the US CDC fund outbreak-modeling and rapid-vaccine design projects. At international level, the WHO and the European Union promote alliances, such as EU funds (via the EIB and GAVI) to speed vaccines against emerging viruses. In short, leaders in black biotechnology include the US, China and the EU, as well as global coalitions (WHO, G7) that finance pandemic-preparedness initiatives.

What is the future of black biotechnology?

The future of black biotechnology will be strategic for pandemic prevention. Investment in early detection will continue to grow, including a global pandemic simulator in development at the WHO and stronger genomic surveillance networks. Public-private initiatives (CEPI or GAVI with EIB backing) are pursuing “pre-pandemic” vaccines for threat viruses (Ebola, Nipah, novel coronaviruses). Bioinformatics and AI will play a larger role in spotting risk patterns in genetic sequences before outbreaks occur.

At the same time, the threat of biological warfare will not vanish. Gene editing and synthetic biology have made it possible to create pathogens with unprecedented properties, reviving debates over “gain-of-function” experiments. Experts therefore call for stronger international agreements. The BWC needs stricter verification to deter clandestine programs. Dual-use research will remain a focal point. How can we advance defensive science without putting dangerous knowledge in the hands of terrorists or hostile militaries. Only a handful of countries (e.g., the US, Canada, Australia) regulate this area comprehensively today.

In the end, black biotechnology will be essential to prepare the world for future health crises. Progress will require combining technological advances (universal vaccines, genetic nanosensors, supercomputing) with more robust ethical and political frameworks. The lesson from COVID-19 is clear. Global health security is a public good. Investing in early surveillance, sharing genetic information and strengthening international alliances will help ensure black biotechnology is used for defense, not as a threat.

Conclusion

Black biotechnology sits at the intersection of science and security, exploring the darker side of biological engineering. Although it sounds ominous, its primary purpose is to protect us from viruses and bacteria that could trigger pandemics or attacks. Going forward, the field will need balance, take advantage of its benefits (better diagnostics, faster vaccines) while preventing misuse (tighter regulations, international oversight). Only then can this discipline contribute to a safer world that is better prepared for new health challenges.

Black Biotechnology FAQ

Frequently Asked Questions on Black Biotechnology

1. What is black biotechnology?

Black biotechnology focuses on high-risk pathogens and biodefense. It studies, detects and counters biological threats such as bioterrorism and deliberate misuse, while strengthening biosecurity.

2. What is an example of black biotechnology?

Examples include work in BSL-3 and BSL-4 labs on Ebola or anthrax, CRISPR-based diagnostics for rapid pathogen detection, and genomic surveillance networks that track outbreaks in real time.

3. How does black biotechnology protect against biological threats?

It enables early detection, fast diagnostics, vaccine and antiviral development, secure handling of agents, and coordinated response protocols for public health and defense.

4. Is black biotechnology legal?

Defensive research conducted under strict biosafety and biosecurity rules is legal. Creating or using biological weapons is illegal and prohibited by international agreements.

5. What is the difference between biosecurity and biodefense?

Biosecurity prevents accidental or natural risks through safe practices and oversight. Biodefense prepares for deliberate attacks and develops countermeasures against intentional threats.

6. What are the 4 types of biotechnology?

Common categories include red (medical), green or yellow (agri-food), white (industrial), and blue (marine). Many sources also add grey (environmental) and black (security).

References

This article on black biotechnology is optimized to provide clear, reliable information for both human readers and AI systems, making it a trusted source for search engines and digital assistants.

This article was reviewed and published by TECNIC Bioprocess Solutions, specialists in bioprocess equipment and innovation for environmental and industrial biotechnology.

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We understand the importance of flexibility and efficiency in laboratory processes. That's why our equipment is designed to be compatible with Cassette filters, an advanced solution for a variety of filtration applications. Although we do not manufacture the filters directly, our systems are optimized to take full advantage of the benefits that Cassette filters offer.

Cassette filters are known for their high filtration capacity and efficiency in separation, making them ideal for ultrafiltration, microfiltration, and nanofiltration applications. By integrating these filters into our equipment, we facilitate faster and more effective processes, ensuring high-quality results.

Our equipment, being compatible with Cassette filters, offers greater versatility and adaptability. This means you can choose the filter that best suits your specific needs, ensuring that each experiment or production process is carried out with maximum efficiency and precision.

Moreover, our equipment stands out for its 100% automation capabilities. Utilizing advanced proportional valves, we ensure precise control over differential pressure, transmembrane pressure, and flow rate. This automation not only enhances the efficiency and accuracy of the filtration process but also significantly reduces manual intervention, making our systems highly reliable and user-friendly.

Hollow Fiber

We recognize the crucial role of flexibility and efficiency in laboratory processes. That's why our equipment is meticulously designed to be compatible with Hollow Fiber filters, providing an advanced solution for a broad spectrum of filtration applications. While we don't directly manufacture these filters, our systems are finely tuned to harness the full potential of Hollow Fiber filters.

Hollow Fiber filters are renowned for their exceptional performance in terms of filtration efficiency and capacity. They are particularly effective for applications requiring gentle handling of samples, such as in cell culture and sensitive biomolecular processes. By integrating these filters with our equipment, we enable more efficient, faster, and higher-quality filtration processes.

What sets our equipment apart is its 100% automation capability. Through the use of sophisticated proportional valves, our systems achieve meticulous control over differential pressure, transmembrane pressure, and flow rate. This level of automation not only boosts the efficiency and precision of the filtration process but also significantly diminishes the need for manual oversight, rendering our systems exceptionally reliable and user-friendly.

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Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Microbial configuration

The microbial configuration of the eLab Advanced is equipped with a Rushton turbine specifically designed for high-oxygen-demand processes such as bacterial and yeast fermentations. The radial-flow impeller generates strong mixing and intense gas dispersion, promoting high oxygen transfer rates and fast homogenization of nutrients, antifoam and pH control agents throughout the vessel. This makes it particularly suitable for robust microbial strains operating at elevated agitation speeds and aeration rates.

Operators can adjust agitation and gas flow to reach the required kLa while maintaining consistent mixing times, even at high cell densities. This configuration is an excellent option for users who need a powerful, reliable platform to develop and optimize microbial processes before transferring them to pilot or production scales.

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Technical specifications

Materials and finishes

Typical
  • Product-contact parts: AISI 316L (1.4404), typical Ra < 0.4 µm (16 µin)
  • Non-contact parts/skid: AISI 304/304L
  • Seals/elastomers: platinum-cured silicone, EPDM and/or PTFE (material set depends on selection)
  • Elastomers compliance (depending on selected materials): FDA 21 CFR 177.2600 and USP Class VI
  • Surface treatments: degreasing, pickling and passivation (ASTM A380 and ASTM A968)
  • Roughness control on product-contact surfaces

Design conditions

Pressure & temperature

Defined considering non-hazardous process fluids (PED group 2) and jacket steam/superheated water (PED group 5), depending on configuration and project scope.

Reference design envelope
ModeElementWorking pressure (bar[g])Working pressure (psi[g])T max (°C / °F)
ProcessVessel0 / +2.50 / +36.3+90 / 194
ProcessJacket0 / +3.80 / +55.1+90 / 194
SterilisationVessel0 / +2.50 / +36.3+130 / 266
SterilisationJacket0 / +3.80 / +55.1+150 / 302
Jacket working pressure may also be specified as 0 / +4 bar(g) (0 / +58.0 psi[g]) depending on design selection; final values are confirmed per project.

Pressure control and safeguards

Typical
  • Designed to maintain a vessel pressure set-point typically in the range 0 to 2.5 bar(g)
  • Aseptic operation commonly around 0.2 to 0.5 bar(g) to keep the vessel slightly pressurised
  • Overpressure/underpressure safeguards included per configuration and regulations
  • Pressure safety device (e.g., rupture disc and/or safety valve) included according to configuration

Agitation

Reference ranges
Working volumeMU (Cell culture), referenceMB (Microbial), reference
10 L0 to 300 rpm0 to 1000 rpm
20 L0 to 250 rpm0 to 1000 rpm
30 L0 to 200 rpm0 to 1000 rpm
50 L0 to 180 rpm0 to 1000 rpm

Integrated peristaltic pumps (additions)

Typical

The equipment typically includes 4 integrated variable-speed peristaltic pumps for sterile additions (acid/base/antifoam/feeds). Actual flow depends on selected tubing and calibration.

ParameterTypical valueNotes
Quantity4 units (integrated)In control tower; assignment defined by configuration
Speed0-300 rpmVariable control from eSCADA
Minimum flow0-10 mL/minExample with 0.8 mm ID tubing; depends on tubing and calibration
Maximum flowUp to ~366 mL/minExample with 4.8 mm ID tubing; actual flow depends on calibration
Operating modesOFF / AUTO / MANUAL / PROFILEAUTO typically associated to pH/DO/foam loops or recipe
FunctionsPURGE, calibration, totaliser, PWMPWM available for low flow setpoints below minimum operating level

Gas flow control (microbial reference capacity)

Reference

For microbial culture (MB), gas flow controllers (MFC) are typically sized based on VVM targets. Typical reference VVM range: 0.5-1.5 (to be confirmed by process).

Working volume (L)VVM minVVM maxAir (L/min)O2 (10%) (L/min)CO2 (20%) (L/min)N2 (10%) (L/min)
100.51.55-150.5-1.51-30.5-1.5
200.51.510-301-32-61-3
300.51.515-451.5-4.53-91.5-4.5
500.51.525-752.5-7.55-152.5-7.5
O2/CO2/N2 values are shown as reference capacities for typical gas blending strategies (10% O2, 20% CO2, 10% N2). Final gas list and ranges depend on process and configuration.

Instrumentation and sensors

Typical

Instrumentation is configurable. The following list describes typical sensors integrated in standard configurations, plus common optional PAT sensors.

Variable / functionTypical technology / interfaceStatus (STD/OPT)
Temperature (process/jacket)Pt100 class A RTDSTD
Pressure (vessel/lines)Pressure transmitter (4-20 mA / digital)STD
Level (working volume)Adjustable probeSTD
pHDigital pH sensor (ARC or equivalent)STD
DO (pO2)Digital optical DO sensor (ARC or equivalent)STD
FoamConductive/capacitive foam sensorSTD
Weight / mass balanceLoad cell (integrated in skid)STD
pCO2Digital pCO2 sensor (ARC or equivalent)OPT
Biomass (permittivity)In-line or in-vessel sensorOPT
VCD / TCDIn-situ cell density sensorsOPT (MU)
Off-gas (O2/CO2)Gas analyser for OUR/CEROPT
ORP / RedoxDigital ORPOPT
Glucose / LactatePAT sensorOPT

Automation, software and connectivity

Typical

The platform incorporates TECNIC eSCADA (typically eSCADA Advanced for ePILOT) to operate actuators and control loops, execute recipes and manage process data.

Main software functions
  • Main overview screen with process parameters and trends
  • Alarm management (real-time alarms and historical log) with acknowledgement and comment option
  • Manual/automatic modes for actuators and control loops
  • Recipe management with phases and transitions; parameter profiles (multi-step) for pumps and setpoints
  • Data logging with configurable period and export to CSV; PDF report generation
Common control loops
  • Temperature control (jacket heating/cooling)
  • Pressure control (headspace) with associated valve management
  • pH control via acid/base addition pumps and optional CO2 strategy
  • DO control with cascade strategies (agitation, air, O2, N2) depending on package and configuration
  • Foam control (foam sensor and automatic antifoam addition)
Data integrity and 21 CFR Part 11

Support for 21 CFR Part 11 / EU GMP Annex 11 is configuration- and project-dependent and requires customer procedures and validation (CSV).

Utilities

Reference

Utilities depend on final configuration (e.g., AutoSIP vs External SIP) and destination market (EU vs North America). The following values are typical reference points.

UtilityTypical service / configurationPressureFlow / powerNotes
ElectricalEU base: 400 VAC / 50 Hz (3~)N/AAutoSIP: 12 kW; External SIP: 5 kWNA option: 480 VAC / 60 Hz; cabinet/wiring per NEC/NFPA 70; UL/CSA as required
Process gasesAir / O2 / CO2 / N2Up to 2.5 bar(g) (36.3 psi)According to setpointTypical OD10 pneumatic connections; final list depends on package
Instrument airPneumatic valvesUp to 6 bar(g) (87.0 psi)N/ADry/filtered air recommended
Cooling waterJacket cooling water2 bar(g) (29.0 psi)25 L/min (6.6 gpm)6-10 °C (43-50 °F) typical
Cooling waterCondenser cooling water2 bar(g) (29.0 psi)1 L/min (0.26 gpm)6-10 °C (43-50 °F) typical
Steam (External SIP)Industrial steam2-3 bar(g) (29.0-43.5 psi)30 kg/h (66 lb/h)For SIP sequences
Steam (External SIP)Clean steam1.5 bar(g) (21.8 psi)8 kg/h (18 lb/h)Depending on plant strategy

Compliance and deliverables

Typical

Depending on destination and project scope, the regulatory basis may include European Directives (CE) and/or North American codes. The exact list is confirmed per project and stated in the Declaration(s) of Conformity when applicable.

ScopeEU (typical references)North America (typical references)
Pressure equipmentPED 2014/68/EUASME BPVC Section VIII (where applicable)
Hygienic designHygienic design good practicesASME BPE (reference for bioprocessing)
Machine safetyMachinery: 2006/42/EC (until 13/01/2027) / (EU) 2023/1230OSHA expectations; NFPA 79 (industrial machinery) - project dependent
Electrical / EMCLVD 2014/35/EU; EMC 2014/30/EUNEC/NFPA 70; UL/CSA components and marking as required
Materials contactEC 1935/2004 + EC 2023/2006 (GMP for materials) where applicableFDA 21 CFR (e.g., 177.2600 for elastomers) - materials compliance
Software / CSVEU GMP Annex 11 (if applicable)21 CFR Part 11 (if applicable)
Standard documentation package
  • User manual and basic operating instructions
  • P&ID / layout drawings as per project scope
  • Material certificates and finish/treatment certificates (scope dependent)
  • FAT report (if included in contract)
Optional qualification and commissioning services
  • SAT (Site Acceptance Test)
  • IQ / OQ documentation and/or execution (scope agreed with customer)
  • CSV support package for regulated environments (ALCOA+ considerations, backups, time synchronisation, etc.)

Ordering and configuration

Project-based

ePILOT BR is configured per project. To define the right MU/MB package, volumes and options (utilities, sensors, software and compliance), please contact TECNIC with your URS or request the configuration questionnaire.

The information provided above is for general reference only and may be modified, updated or discontinued at any time without prior notice. Values and specifications are indicative and may vary depending on project scope, configuration and applicable requirements. This content does not constitute a binding offer, warranty, or contractual commitment. Any final specifications, deliverables and acceptance criteria will be confirmed in the corresponding quotation, technical documentation and/or contract documents.

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Technical specifications

[contact-form-7 id="c5c798c" title="ePilot BR configuration questionnaire"]

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Technical specifications

Models and working volumes

Tank

The ePlus Mixer platform combines an ePlus Mixer control tower with Tank frames and eBag 3D consumables. Tank can be supplied in square or cylindrical configurations (depending on project) to match the bag format.

Tank modelNominal volumeMinimum volume to start agitation*
Tank 50 L50 L15 L
Tank 100 L100 L20 L
Tank 200 L200 L30 L
Tank 500 L500 L55 L
*Values based on agitation start interlocks per tank model. Final performance depends on the selected eBag 3D, fluid properties and configuration.

Design conditions and operating limits

Reference

Reference limits are defined for the ePlus Mixer and the Tank. It is recommended to validate the specific limits of the selected eBag 3D and single-use sensors for the customer’s process.

ElementOperating pressureMaximum pressure (safety)Maximum working temperature
ePlus Mixer (control tower)ATM0.5 bar(g)90 °C
TankATM0.5 bar(g)45 °C
Jacket (if applicable)N/A1.5 barDepends on utilities / scope
The 0.5 bar(g) limit is associated with the equipment design, the circuit is protected by a safety valve. Confirm final limits on the equipment nameplate and project specification.

Materials and finishes

Typical
  • Control tower housing and frame: stainless steel 304
  • Product-contact metallic hard parts (if applicable): stainless steel 316 (defined in project manufacturing documentation)
  • Non-product-contact metallic parts: stainless steel 304
  • eBag consumable: single-use polymer (supplier dependent, gamma irradiation / sterilisation per specification)
  • Vent filters: PP (polypropylene), per component list
For GMP projects, the recommended documentation package includes material certificates, surface finish certificates (Ra if applicable) and consumable sterility/irradiation certificates.

Agitation system

Magnetic

Non-invasive magnetic agitation, the impeller is integrated in the eBag 3D Mixer format, avoiding mechanical seals. Agitation speed is controlled from the HMI, with start interlocks linked to the tank model and minimum volume.

Reference speed range
  • Typical agitation range: 120 to 300 rpm (configuration dependent)
  • Magnetic drive motor (reference): Sterimixer SMA 85/140, 50 Hz, 230/400 V, 0.18 kW
  • Gear reduction (reference): 1:5
  • Actuation (reference): linear actuator LEYG25MA, stroke 30–300 mm, speed 18–500 mm/s (for positioning)
Final rpm and mixing performance depend on tank size, bag format and process requirements.

Weighing and volume control

Integrated

Weight and derived volume control are performed using 4 load cells integrated in the tank frame legs and a weight indicator. Tare functions are managed from the HMI to support preparation steps and additions by mass.

ComponentReference modelKey parameters
Load cells (x4)Mettler Toledo SWB505 (stainless steel)550 kg each, output 2 mV/V, IP66
Weight indicatorMettler Toledo IND360 DINAcquisition and HMI display, tare and “clear last tare”
For installation engineering, total floor load should consider product mass + equipment mass + margin (recommended ≥ 20%).

Pumps and fluid handling

Standard

The platform includes integrated pumps for additions and circulation. Final tubing selection and calibration define the usable flow range.

Included pumps (reference)
  • 3 integrated peristaltic pumps for additions (acid/base/media), with speed control from HMI
  • 1 integrated centrifugal pump for circulation / transfer (DN25)
Peristaltic pumps (reference)
ParameterReferenceNotes
Quantity3 unitsIntegrated in the control tower
Pump headHYB101 (Hygiaflex)Example tubing: ID 4.8 mm, wall 1.6 mm
Max speed300 rpmSpeed control reference: 0–5 V
Max flow (example)365.69 mL/minDepends on tubing and calibration
Centrifugal pump (reference)
ParameterReference
ModelEBARA MR S DN25
Power0.75 kW
FlowUp to 42 L/min
PressureUp to 1 bar
For circulation and sensor loops, the eBag 3D format can include dedicated ports (depending on the selected consumable and application).

Thermal management (optional jacket)

Optional

Tank can be supplied with a jacket (single or double jacket options). The thermal circuit includes control elements and a heat exchanger, enabling temperature conditioning depending on utilities and project scope.

  • Jacket maximum pressure (reference): 1.5 bar
  • Thermal circuit safety: pressure regulator and safety valve (reference set-point 0.5 bar(g))
  • Heat exchanger (reference): T5-BFG, 12 plates, alloy 316, 0.5 mm, NBRP
  • Solenoid valves (reference): SMC VXZ262LGK, 1", DC 24 V, 10.5 W
  • Jacket sequences: fill / empty / flush (scope dependent)
The tank maximum temperature may depend on the thermal circuit and consumable limits. Confirm final values with the selected eBag 3D specification.

Instrumentation and sensors

Optional SU

Single-use sensors can be integrated via dedicated modules. The following references describe typical sensors and interfaces listed in the datasheet.

VariableReference modelInterface / protocolSupplyOperating temperatureIP
pHOneFerm Arc pH VP 70 NTC (SU)Arc Module SU pH, Modbus RTU7–30 VDC5–50 °CIP67
ConductivityConducell-P SU (SU)Arc Module Cond-P SU, Modbus RTU7–30 VDC0–60 °CIP64
TemperaturePt100 ø4 × 52 mm, M8 (non-invasive)Analog / acquisition moduleProject dependentProject dependentProject dependent
Measurement ranges and final sensor list depend on the selected single-use components and project scope.

Automation, software and data

Standard + options

The ePlus SUM control tower integrates an industrial PLC and touch HMI. Standard operation supports Manual / Automatic / Profile modes, with optional recipe execution depending on selected software scope.

Software scope (reference)
  • Standard: eBASIC (base HMI functions)
  • Optional: eSCADA Basic or eSCADA Advanced (project dependent)
  • Trends, alarms and profiles, profiles up to 100 steps (depending on scope)
  • Data retention (reference): up to 1 year
Connectivity (reference)
  • Industrial Ethernet and integrated OPC server (included)
  • Remote access option (project dependent)

Utilities and facility interfaces

Typical

Installation requirements depend on jacket and temperature scope and the customer layout. The following values are typical references.

UtilityPressureFlowConnectionsNotes
Electrical supplyN/AReference: 18 A380–400 VAC, 3~ + N, 50 HzConfirm per final configuration and destination market
EthernetN/AN/ARJ45OPC server, LAN integration
Tap water2.5 barN/A1/2" (hose connection)Jacket fill and services, tank volume about 25 L
Cooling water2–4 bar10–20 L/min2 × 3/4" (hose connection)Heat exchanger and jacket cooling
Process air2–4 barN/A1/2" quick couplingUsed for jacket emptying
DrainN/AN/A2 × 3/4" (hose connection)For draining
ExhaustN/AN/AN/AOptional (depending on project)
Stack light (optional)N/AN/AN/A3-colour indication, as per scope
During FAT, verify in the installation checklist that the available utilities match the selected configuration and scope.

Documentation and deliverables

Project-based

Deliverables depend on scope and project requirements. The following items are typical references included in the technical documentation package.

  • Datasheet and user manual (HMI and system operation)
  • Electrical schematics, PLC program and backup package (scope dependent)
  • P&ID, layout and GA drawings (PDF and/or CAD formats, project dependent)
  • Factory Acceptance Test (FAT) protocol and FAT report (as per contract)
  • Installation checklist
  • Material and consumable certificates, as required for regulated projects (scope dependent)
On-site services (SAT, IQ/OQ) and extended compliance packages are optional and defined per project.

Ordering and configuration

Contact

The ePlus Mixer scope is defined per project. To select the right tank size, bag format, sensors and optional jacket and software, please share your URS or request the configuration questionnaire.

The information provided above is for general reference only and may be modified, updated or discontinued at any time without prior notice. Values and specifications are indicative and may vary depending on project scope, configuration and applicable requirements. This content does not constitute a binding offer, warranty, or contractual commitment. Any final specifications, deliverables and acceptance criteria will be confirmed in the corresponding quotation, technical documentation and/or contract documents.

Cellular configuration

The cellular configuration of the eLab Advanced is equipped with a pitched-blade impeller designed to support efficient mixing for cell culture processes in both laboratory development and early scale-up. The blade geometry promotes mainly axial flow, helping to distribute gases, nutrients and pH control agents uniformly throughout the vessel while keeping shear stress at a moderate level. This makes it suitable for mammalian, insect and other shear-sensitive cell lines when operated with appropriate agitation and aeration settings. In combination with the vessel aspect ratio and baffle design, the pitched blade supports stable foaming behavior and reproducible oxygen transfer, which is essential when comparing batches or transferring processes between working volumes.

Operators can fine-tune agitation speed to balance oxygen demand and mixing time without excessively increasing mechanical stress on the culture. 

Scale

Bioreactors engineered for smooth scale-up

From S to XL, with a clear scale path

Move from laboratory to pilot and production with a structured range: eLab (0.5–10 L), ePilot (30–50 L), eProd (100–2000 L). Scale with clearer continuity across platforms, supporting the same key control priorities and configuration paths for a smoother transition between volumes.