Büchner filters for liquid/solid separation in the Pharmaceutical sector
Büchner CLA filters are custom designed for liquid/solid separation in pharmaceutical processes requiring purity, traceability and GMP compliance. Using a static filter mesh, these filters effectively separate the liquid and solid phases by pressurizing the chamber, ensuring reliable results for the production of active ingredients, intermediates or sterile solutions.
Specifications
- Custom-designed static filter mesh for efficient separation of liquid and solid phase.
- Pressure operation: the solution is pushed into the filter chamber, resulting in homogeneous and safe separation.
- Stainless steel construction suitable for pharmaceutical processes, easily washed and conforms to GMP standards.
- Easy opening and cleaning: quick access for solid extraction and sanitization between batches, can be integrated with CIP/SIP.
- Custom configuration: capacity, diameter, materials and safety systems made according to the department’s needs.
- Complete technical documentation: material certifications, drawings, IQ/OQ and regulatory audit support.
Typical applications in pharmaceuticals
- Liquid/solid separation of active suspensions, synthetic intermediatesî, sterile products and solutions with a need for batch tracing and traceability.
- Recovery of active ingredients or filters in processes requiring purity and GMP compliance.
- Pilot and industrial production, with customized filter configuration of each batch.
Strengths
- Full customization: capacity, materials and design upon request.
- Rapid sanitization, ease of cleaning, and compatibility with CIP/SIP systems.
- IQ/OQ certification, traceability and document support for GMP audits.
- Easy integration with other existing CLA plants or pharmaceutical lines.
- Dedicated service: consulting, design, installation and after-sales support.
Request your pharmaceutical Büchner filter now.
FAQ – Büchner pharmaceuticals CLA filters.
What capabilities are available?
Custom solutions, from laboratory to production batch, according to the pharmaceutical process.
Is the filter suitable for sterile processes?
Yes, designed for washability, sanitizability and GMP materials.
How does liquid/solid separation work?
The product is put under pressure, and the net holds back the solid, letting the liquid part pass through.
Is it easy to clean between batches?
Yes, quick opening, direct access, and CIP/SIP washing capability.
Do I receive documentation for audits?
Yes: materials, technical drawings, IQ/OQ and GMP audit documents.