Frequently asked questions in biotechnology

Yes, all our services are designed to suit your specific plant and product requirements. From equipment design to system integration, we ensure that each solution is unique.

Our team will conduct a detailed assessment of your current processes to identify opportunities for improvement in efficiency, safety and compliance.

We cover everything from bioprocess design and automation to the production of purified water and CIP cleaning systems, always with a focus on operational and regulatory optimisation.

From conceptual engineering to turnkey projects, we offer complete solutions for the biopharmaceutical and biotechnology industry. We specialise in qualification, validation and optimisation of industrial processes, always ensuring the strictest regulatory compliance.

Of course you can. Although our end-to-end approach is highly efficient, we can work on specific phases of your project as needed.

First we analyse your needs and develop a customised technical proposal. Once approved, we start planning and executing the project, maintaining constant communication at every stage.

We deliver validated and documented processes that comply with all international standards, backed by an expert technical team that ensures measurable results.

Depending on the complexity, this can vary. We will provide you with a detailed timeline at the beginning of the project so that you are aware of every step.

Yes, we prepare all necessary documentation and protocols for regulatory audits. Our goal is to ensure that your plant passes any assessment without any problems.

From technical training to immediate assistance in case of problems, our after-sales service ensures that you continue to achieve optimal results even after the end of the project.

Thanks to our experience, we anticipate potential risks and adjust action plans to minimise disruptions. In addition, our team will be at your side to solve any problems that may arise.

We offer ongoing technical support, system upgrades and preventive maintenance to ensure that your equipment and processes are always running at peak performance.

Yes, we use components and materials from globally recognised brands, selected for their durability, reliability and regulatory compliance.

We validate each stage and component through protocols such as FAT, SAT, IQ and OQ, ensuring that processes are consistent batch after batch.

Our specialisation in bioprocesses and our ability to customise each solution position us as a leader in the sector. In addition, we deliver reproducible and documented results that facilitate audits and ensure consistency.

We comply with GMP, FDA, ASME BPE and GAMP 5, among others. In addition, we apply tools such as FMEA analysis and the Quality Risk Matrix to ensure that everything is aligned with the highest standards.

From initial design to execution, we are guided by the strictest international regulations. In addition, we provide comprehensive documentation to support each process.

Yes, we offer system upgrade and enhancement services to ensure that your installations always comply with the latest standards.

Our support team is available to solve any problem. In addition, we have a preventive maintenance service to minimise risk.

We include operating manuals, quality certificates, validation protocols and detailed technical diagrams. This ensures that you have everything you need for audits and future operation.