Cleaning Validation

At QbD Group, we provide comprehensive Cleaning Validation services customized to meet the specific requirements of your industry and regulatory requirements. 

Our team uses advanced methods to ensure your cleaning procedures meet strict efficiency and regulatory standards. 

Don’t hesitate to contact us for more information.

Cleaning Validation

What is Cleaning Validation?

FROM DESIGN TO PERFORMANCE QUALIFICATION

Cleaning Validation is the process of confirming that cleaning procedures effectively and reproducibly remove residues and contaminants from equipment surfaces used in manufacturing processes. It involves systematic testing and documentation to ensure that cleaning methods consistently meet predetermined standards and regulatory requirements. 

Cleaning validation does not only contribute to the safety and efficacy  of medicinal products, it also helps to be compliant with regulations, reduce your production costs and improve the robustness and efficiency of your manufacturing process. It helps to determine the worst case and risks that may arise during the manufacturing of the quality products. 

Cleaning Validation Essential to ensure:

  • Product Quality: Proper cleaning validation ensures that your equipment is free from residues that could contaminate subsequent batches of your products, maintaining product purity and quality. 
  • Regulatory Compliance: Regulatory agencies require cleaning validation to ensure that manufacturing processes adhere to safety and quality standards, reducing the risk of product recalls or regulatory sanctions. 
  • Patient Safety: In industries such as pharmaceuticals and healthcare, cleaning validation is crucial for preventing cross-contamination and ensuring patient safety by eliminating the risk of exposure to harmful residues. 
  • Process Efficiency: Effective cleaning validation minimizes the risk of equipment malfunction or product contamination, reducing downtime and optimizing production efficiency. 

Why QbD Group?

YOUR EXPERT IN C&Q AND EQUIPMENT VALIDATION

During the C&Q portion of your project, clear and pragmatic project direction and execution are the first steps to a well-executed project.

Our expert support enables you to reduce the overall cost of your project. Pragmatism, right first time, and leverage are part of our DNA. 

Equipment Validation - Quality by Design

Tailored solutions

FLEXIBLE SERVICE

You can choose a fully turnkey solution with project management by QbD, or a hybrid solution where the project management is done by your company and the rest is managed by QbD.

Contact us

TALK TO AN EXPERT

Don’t hesitate to contact us so we can listen to your needs and provide you with the right C&Q and/or equipment validation service.

Come visit our booth at CPHI Barcelona 2023

Come to see the QbD Group at stand #3G73 at CPHI Conference in Barcelona. And after the conference…Eat & Connect with lifescience professionals at our QbD’s CPHI Networking Drink.