Creative Biolabs offers high-standard quality assurance (QA) service strictly following established Quality Systems, compliant with most international regulations. Our QA service aims at improving and stabilizing production and associated processes to avoid issues leading to defects. Our professionally trained scientist team provides comprehensive and systematic activities to assure the consistent quality of our customers’ products. In addition, our QA service includes a wide range of organized procedures, which covers all matters that individually or collectively influence the quality of products and ensures that the safety, integrity and quality of released products conform to cGMP. GMP is the part of QA system that ensures the products are of consistent quality under fully controlled quality standards, meeting the strictest FDA and USP guidelines.
Creative Biolabs is most concerned with diminishing the risks inherent in any pharmaceutical production due to inadequate safety, quality or efficacy; we are ready to assist with any questions our customers may have about QA requirements ranging from clinical trials to commercial manufacturing.
Our QA service including but not limited to:
Monitoring outsourced activities (contract analysis and manufacturing)
Monitoring suppliers and subcontractors
Raw materials release
Products release
cGMP trainings
Review and approval of validation protocols
Equipment and facilities compliance with cGMP
SOP review and approval
Comprehensive quality system design
Comprehensive quality system documented
Comprehensive quality system implemented
To discuss your QA Service demands or to request a proposal, please contact us.
For Research Use Only. Not For Clinical Use.
