CIP Solutions for Biopharmaceutical Manufacturing
Cleaning-in-place (CIP) solutions are crucial for maintaining the highest standards of quality, safety, and efficiency in biopharmaceutical production—especially during downstream processing, where products are separated and purified after fermentation.
Key benefits and features
- 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 (PQD), supporting your validation and qualification processes.
CIP Solutions:
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: Optimizes cleaning cycles to save water and chemicals.
- Regulatory Compliance: Supports validated, consistent cleaning to meet industry standards.
- Risk Mitigation: Minimizes microbial growth and biofilm formation.
- Time Savings: Cuts manual labor and speeds up batch turnover.
- Validation & Documentation: Enables standardized, traceable processes for audits.
PORTFOLIO OF GMP COMPLIANT CLEANING-IN-PLACE (CIP) SOLUTIONS
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 (WfI), and are rigorously tested to meet EP and USP standards.
As the industry moves towards single-use systems, ready-to-use CIP solutions—pre-adjusted to the required concentration—offer added convenience. Each product is supported by a comprehensive Product Qualification Dossier (PQD) to assist with validation and qualification.
PharmProve® Portfolio (extract)
| 2-Propanol 70 % | Sodium hydroxide solution 1M PharmProve® Plus |
| Acetic acid (glacial) 99 %/100 % EP, USP, JP PharmProve® | Sodium hydroxide solution 10M PharmProve® Plus |
| Ethanol 20 % w/w PharmProve® Plus | Sodium hydroxide solution 45 % PharmProve® Plus |
| Sodium chloride solution 1M PharmProve® Plus | Phosphoric acid 85 % EP, BP, USP PharmProve® |
| Sodium chloride solution 3M PharmProve® Plus | Hydrochloric acid 1M PharmProve® Plus |
| Sodium chloride solution 4M PharmProve® Plus | Hydrochloric acid 2M PharmProve® Plus |
| Sodium chloride solution 5M PharmProve® Plus | Hydrochloric acid 37 % EP, USP, JP PharmProve® |
| Sodium hydroxide solution 0.1M PharmProve® Plus | Citric acid solution 50 % PharmProve® Plus |
| Sodium hydroxide solution 0.5M PharmProve® Plus |
Our Experts For you
Our Experts - Your Partners
Overview of key contacts - supported by many more specialists working for our partners and Clients behind the scenes.
Dr. Frank Velte
Head of CG Pharma & Biotech
+49 (0)511 87803-106
+49 (0)152 3466 7631
frank.velte@cg-chemikalien.de
Marco Regel
Head of Sales & Business Development
+49 (0)511 / 87803-146
+49(0)511 / 2516696
marco.regel@cg-chemikalien.de
Thomas Metzger
Sales & Business Development Manager
+49 (0)511 87803-258
+49 (0)79 483 72 81
thomas.metzger@cg-chemikalien.de
