CIP Solutions for Biopharmaceutical Manufacturing
Cleaning in place (CIP) solutions are crucial in biologics manufacturing because they enable thorough and consistent cleaning of equipment without disassembly. This reduces the risk of contamination and cross-contamination between production batches.
As a result, CIP supports compliance with strict regulatory standards and ensures product safety.
- Effective cleaning: Ensure thorough removal of product residues and microbiological contaminants from production equipment, supporting reliable and safe manufacturing processes.
- GMP-certified production: All CIP solutions are manufactured in our GMP-certified facility in Germany, guaranteeing consistent quality and compliance.
- High-quality raw materials: Only raw materials from accredited sources are used, with each batch rigorously tested for identity and quality in accordance with EP and USP standards.
- Water for injection (WFI): Our cleaning solutions are prepared using specially produced water for injection, ensuring maximum purity.
- Ready-to-use convenience: As the industry shifts towards single-use equipment, our ready-to-use CIP solutions – pre-adjusted to the required end concentration – offer time and cost savings.
- Comprehensive documentation: Each product is supplied with a detailed product qualification dossier, supporting your validation and qualification processes.
Key to achieving the highest quality standards
Cleaning in place (CIP) solutions are essential for ensuring quality, safety and efficiency in biopharmaceutical production, particularly during downstream processing where products are separated and purified.
Key benefits of CIP solutions:
- Product quality: Prevents cross-contamination and ensures product purity.
- Process efficiency: Automates cleaning, reduces downtime and boosts productivity.
- Resource conservation: Optimises cleaning cycles to save water and chemicals.
- Regulatory compliance: Supports validated, consistent cleaning to meet industry standards.
- Risk mitigation: Minimises microbial growth and biofilm formation.
- Time savings: Cuts manual labour and speeds up batch turnover.
- Validation and documentation: Enables standardised, traceable processes for audits.
We offer tailored CIP solutions and catalogue items that reliably remove product residues and microbiological contaminants from equipment. Manufactured in a GMP-certified facility in Germany, these solutions use high-quality raw materials and water for injection and are rigorously tested to meet EP and USP standards.
Portfolio of GMP-Compliant Cleaning-in-place Solutions
PRODUCTS | |
|---|---|
Acetic acid (glacial) 99%/100% EP, USP, JP PharmProve® | Phosphoric acid 85% EP, BP, USP PharmProve® |
Citric acid solution 50% PharmProve® Plus | Sodium hydroxide solution 0.1M PharmProve® Plus |
Ethanol 20% w/w PharmProve® Plus | Sodium hydroxide solution 0.5M PharmProve® Plus |
Hydrochloric acid 1M PharmProve® Plus | Sodium hydroxide solution 1M PharmProve® Plus |
Hydrochloric acid 2M PharmProve® Plus | Sodium hydroxide solution 10M PharmProve® Plus |
Hydrochloric acid 37% EP, USP, JP PharmProve® | Sodium hydroxide solution 45% PharmProve® Plus |
