Pharmaceuticals, Biologics

Expert SteriPro® consultants are available to assist pharmaceutical and biologic manufacturers in developing the most cost-effective, long-term sterilization solutions for their products.

Areas of specialization in the pharmaceutical sterilization program include:

• Materials selection and biocompatibility issues
• Process, materials and package validation
• Sterility and quality assurance
• Audit and release testing
• Regulatory consulting

Among those most likely to benefit from SteriPro Consulting services are:

• Manufacturers who desire to profit from the significant cost and time savings offered by terminal sterilization vs. conventional aseptic manufacturing
• Those who wish to realize a better quantification of SAL by supplementing their existing aseptic manufacturing with terminal sterilization
• Small or start-up manufacturers who lack the staff to perform the sterilization studies required to get a product to clinical trial or to accelerate product to market
• Those with limited SA/QA personnel, limited technical resources, or those who cannot afford the time needed to support the sterilization process

To learn more:

Please contact us to discuss the design and implementation of a custom program to meet your pharmaceutical sterilization needs.