Audit Service Center Upgraded at www.auditservicecenter.com

comes compliance services (CCS) has upgraded its audit management services on a seperate domain: www.auditservicecenter.com

The new web site contains an entire overview of the audit management and related tools, which are totally integrated in the process work flows provided by CCS.

The Audit Service Center (ASC) is an independent provider of value-added regulatory quality and audit management services. Starting with the existing compliance programs of our clients we optimize such programs and manage quality audits of manufacturers of materials, products, components, and services providers, in GMP, GCP, GDP, GLP regulated industries such as pharmaceuticals, biologics, medical devices, cosmetics, dietary supplements.

Our team of highly dedicated quality experts delivers to our clients actionable strategic decision systems, improved supply chain processes and inspection readiness. The Audit Service Center implements tested and proven strategies, tools and methods to cut costs and increase profitability of  compliance and audit programs.

Our compliance projects ensure that supply chain requirements meet quality management support, be it for finding a second source of material or component supply, collaborating with suppliers on quality aspects, or investigating suitable outsourcing options. We create the “vendor to partner” dynamics required for improving products and reducing deficiencies.   

Visit now:  www.auditservicecenter.com to get more information and news about audit and CAPA management, supplier chain optimization, shared audits, and other compliance service options.

MS Sharepoint: GMP compliant document & quality management system

comes compliance services offers a new and GMP compliant Document and Quality Management System on the basis of MS Sharepoint. The product from the CCS Partner GxPi provides a well structured and unique document management platform including full audit trail, pre-defined document workflows, version and status control, electronic and digital signature technology, and additional compliance management modules. This 21 CFR Part 11 compliant system can be used for CAPA, OOS, deviation, investigation, and change control management. The MS look and feel makes the system easy to operate in a well known user interface.

Please contact us for more information or a  free web demo at: talk@comes-compliance.com

The one and only full GMP compliant DMS and QMS solution on MS Sharepoint.