Solutions - Cleaning Development
A comprehensive equipment cleaning process and cleaning validation assurance is an important aspect of Performance Qualification (PQ) and is required in the regulatory submission necessary for EMEA and FDA approval.
Our Specialists are an invaluable resource in developing and optimizing your cleaning and sterilization validation program. Our specialists have experience authoring and executing Clean in Place (CIP), Clean Out of Place (COP) and Steam in Place (SIP) protocols. Our specialists also identify cost-saving measures by developing and performing bench-scale guidance studies that can be scaled up to process conditions.
Our cleaning and sterilization services include:
- Drafting and implementing comprehensive equipment cleaning process, design and validation
- Clean Hold Study protocol generation and execution
- Engineered cleaning process improvements implicit to successful operation
- Implementing cleaning chemistry changes