Services
At Becarv, we offer more than just equipment.
We leverage our extensive expertise to provide tailored solutions that integrate seamlessly into your operations, whether in the biopharmaceutical, chemical or healthcare industries. Our focus is on meeting the highest quality standards and ensuring full regulatory compliance, all while aligning with your strategic and operational objectives. Our process is collaborative, starting with a deep understanding of your project’s scope. Whether you are working on a new cleanroom build, upgrading a chemical reactor system, or revamping a production line or controlled storage area to meet regulatory standards like Eudralex Annex 1 Volume 4, we collaborate closely with you to design and implement solutions that drive long-term success.
By partnering from design to ongoing support, we forge long-term relationships that help you stay ahead of both technological and regulatory challenges.

Tailored Solutions & Expert Guidance
We start by engaging in detailed discussions to understand your goals, challenges, and specific needs. This allows us to propose the most suitable technical solutions for your sterile manufacturing areas, sensitive surgical environments, or chemical processing facilities. We then evaluate your existing setup using “as-built” blueprints (or other documentation), which help us determine how our modular solutions can be effectively implemented.
Next, our design and engineering teams conduct an on-site visit to assess your facility’s layout, take precise measurements, and identify any physical constraints (e.g., low ceilings, structural beams) that could impact installation. These insights enable us to refine technical specifications, adjusting them where necessary, such as optimizing ventilation systems or installing air filtration units (e.g., in cleanrooms, ICUs, or chemical distillation units) and around hazardous materials. This ensures seamless integration, minimizes disruption, and prevents surprises during installation.
Key services include:
- Expert knowledge on equipment selection and adaptation to bioprocessing facility constraints, plant safety protocols, and hospital sterile environments.
- On-site assessments, including measurements and layout evaluations.
- Support to ensure regulatory compliance and operational efficiency in biopharmaceutical, chemical, and healthcare sectors.

Design and Manufacturing
At Becarv, we ensure every piece of equipment is designed and built to meet your specifications and operational requirements. Our process is collaborative and thorough, with continuous communication between our teams and yours, ensuring seamless integration into your facility.
Design & Engineering
Once the solution is defined and the order is placed, our design and engineering teams prepare the equipment file and manufacturing plan, capturing all technical details and specifications. We then proceed with manufacturing at our Rochefort workshop, adhering to ISO-9001:15 standards.
Factory Acceptance Testing (FAT)
As part of our qualification process, we follow the ASTM E2500 verification approach to ensure the equipment’s reliability and consistency. Before shipping, all equipment undergoes Factory Acceptance Testing (FAT) at our Rochefort workshop. This critical phase includes performance checks, functional testing, safety validation, and compliance with industry standards. The FAT process ensures that the equipment meets all specifications and is ready for deployment to cleanrooms, chemical plants, and hospital surgical suites. The results are fully documented and included in the validation package.
Key services during the Design & Manufacturing process include:
- Tailored design and engineering of equipment for biopharmaceutical, chemical, and healthcare applications
- Factory Acceptance Testing to validate performance, safety, and functionality in accordance with industry regulations.
- Comprehensive documentation for validation and compliance
Installation & Commissioning
Once FAT is completed and the equipment is cleared for deployment, we proceed with installation and commissioning at your facility, ensuring full compliance with cleanroom protocols for biopharmaceutical environments or chemical safety standards. Our skilled technicians ensure precise setup and full integration into your infrastructure, adhering to strict contamination control standards that are critical for biopharmaceutical manufacturing, hospital settings, and chemical production environments.
Pre-Installation & Site Assessment
Before installation, our team conducts a pre-installation site assessment to evaluate your facility’s layout and identify any unforeseen constraints that could affect the installation of equipment.
Delivery & Installation
Our cleanroom-trained technicians manage delivery, unpacking, and setup, following contamination control protocols to ensure precise equipment installation with minimal disruption to operations.
Site Acceptance Testing (SAT)
After installation, we conduct Site Acceptance Testing (SAT) to ensure the equipment performs as expected in the real-world operating environment. We perform system checks, including mechanical and functional aspects such as laminarity, filter integrity, and integration with existing systems. Adjustments are made to accommodate local conditions and ensure optimal performance for chemical reactors, surgical operating rooms, or biopharmaceutical production areas.
Training & Handover
During commissioning, we provide comprehensive training for your team on the safe and effective operation and maintenance of the equipment, ensuring long-term efficiency and regulatory compliance in your production areas, laboratories, or hospital units.
Key services during the Installation & Commissioning process include:
- On-site project management and coordination for seamless installation
- Equipment setup for biopharmaceutical manufacturing, chemical safety, and healthcare environments
- Site Acceptance Testing
- Comprehensive training for your team on operational safety in manufacturing environments and healthcare facilities.
With precise installation and thorough qualification, we ensure your systems integrate seamlessly into your facility, maximizing operational efficiency and regulatory compliance.

Ongoing Support and Maintenance
At Becarv, our commitment to your success continues well beyond installation and commissioning. We understand that maintaining smooth equipment operation is critical to your facility’s productivity, whether in a biopharmaceutical manufacturing facility, a chemical processing plant, or a healthcare environment. That is why we provide a comprehensive range of maintenance and assistance services to ensure your systems stay dependable, efficient, and compliant throughout their lifecycle. Our initiative-taking and flexible service is tailored to your needs—whether through scheduled maintenance, emergency repairs, or system upgrades as your production demands evolve.
To further enhance reliability, we offer Service Level Agreements (SLAs) that define response times, uptime expectations, and services, ensuring that your needs are addressed promptly with the highest quality.
Maintenance Services
To keep your equipment at peak performance, we offer the following services:
- Scheduled Preventive Maintenance: Regular visits to assess performance and identify potential issues before they affect production in cleanrooms, chemical reactors, or ICUs.
- On-Demand Technical Support: Quick troubleshooting, either remotely or on-site, minimizing downtime in critical areas such as biopharmaceutical production or medical gas systems.
- 24/7 Emergency Service: Round-the-clock service for urgent issues, ensuring continuity of operations in high-risk areas like biopharmaceutical cleanrooms or chemical plant operations.
- Spare Parts Management: Critical spare parts in stock for rapid replacement.
- Troubleshooting and Diagnostics: Fast and effective resolution to prevent disruptions in production lines, hospitals, or chemical facilities.
Upgrades and System Optimization
As your production environment evolves, we assist with upgrades and optimizations to accommodate new needs, regulatory changes, or technological advancements. We help enhance your systems to improve performance, efficiency, and compliance with industry standards for biopharmaceutical, chemical, and healthcare environments.
With ongoing performance and reliability, Becarv remains your trusted partner, supporting you every step of the way to achieve operational excellence and help your business adapt and grow over time.
Regulatory Compliance
In the biopharmaceutical industry, regulatory compliance is paramount, especially for sterile manufacturing environments. At Becarv, we ensure our products and services meet the latest industry regulations for cleanrooms and controlled environments, helping you stay aligned with standards like Eudralex Annex 1 for biopharmaceutical manufacturing, GMP guidelines, USP 979 for sterile drug products, and environmental regulations for the chemical industry.
Our team stays updated on evolving regulatory requirements to guide you through every step of the compliance process. Whether it is during design or in ongoing operations, we help ensure your systems remain compliant with local and international standards.
Our regulatory compliance services include:
- Design and specification to meet GMP, FDA, and industry standards specific to sterile environments, chemical plants, and hospital settings.
- Documentation and certification support
- Ongoing compliance updates and checks
By working closely together from design through to ongoing support, we forge long-term partnerships that help you stay ahead of both technological and regulatory challenges in the biopharmaceutical, chemical, and healthcare industries.
Throughout the lifecycle of your system, Becarv stands by your side to ensure continued compliance with evolving regulations, offering updates and proactive guidance to keep your operations in line with global standards.
Why Chose Becarv?
Trusted Partner in Biopharmaceutical, Chemical, and Healthcare Industries
Becarv is committed to delivering state-of-the-art containment, airflow, and contamination control solutions that meet the highest industry standards.