Converting Biophile Laboratories takes strigent care to maintain the quality level of their Controlled Rooms. Controlled environment manufacturing means that the products created, assembled and packaged are done with the highest standards the medical community demands. Our "controlled" environments assure that your products meet these stringent quality standards.
CONTROLLED ENVIRONMENT MANUFACTURING AND QUALITY ASSURANCE
Converting Biophile Laboratories is a premiere leader in customer satisfaction within our industry by providing the highest quality products and services. We conduct our business according to the highest ethical standards and manage our business for growth and fiscal responsibility.
CUSTOMER SATISFACTION
Customer satisfaction is our most important objective. Our daily decisions and activities must continually serve this goal. All of our staff serve customers - both internal customers and external customers.
CONTINUOUS QUALITY IMPROVEMENT
Continuous quality improvement is everyone's responsibility. Being satisfied with the status quo is completely unacceptable at CBL. The only way we can gauge our improvements is to measure our progress towards attaining and surpassing customer satisfaction goals.
PEOPLE ARE OUR MOST IMPORTANT ASSET
We treat each of our team members and customers with respect and trust. To keep our internal resource competitive, we understand the value of continually developing our skills to enhance our individual productivity and providing opportunities for personal career growth.
Every person at CBL is trained and empowered
to identify quality. This philosophy promotes a supportive team effort to ensure that our standards are upheld across the manufacturing, assembly and packaging processes, including the review of vendor-supplied components.
- Controlled Environment Manufacturing
- ISO 13485 Guidelines
CONTROLLED ENVIRONMENT NEWS
CONTROLLED ROOM REQUIREMENTS
Many medical device and pharmaceutical components require manufacturing and testing in a controlled environment. These pharmaceutical, medical device and industrial manufacturers are constantly looking for ways to reduce the number of contaminants that come in contact with their products. The 3 major sources of particle contamination include supply air, infiltration air and internal generation. Controlled Environment Technology: Fundamentals of design, testing and operation, by W. Whyte
Converting Biophile Laboratories Inc. is a qualified supplier to the Medical Device Industry (QMED)
CONTROLLED ROOM MANUFACTURING AND ASSEMBLY
A recent article in Medical Product Manufacturing News (January 12, 2010) addressed the importance of evaluating your prospective partners for controlled environment technology by considering three factors: the contractor's standards, flexibility, and ability to take the lead in the entire manufacturing process.
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ENVIRONMENTAL MONITORING – Maintaining a Controlled Environment
Featured in Pharm Pro Magazine, this May 28, 2010 article recognized the industry's need to monitor the environmental conditions in aeseptic manufacturing areas.
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