Certified Compliance Solutions
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Description: CCS is a software and process verification and validation provider for the medical device and pharmaceutical industries.
Certified Compliance Solutions, Inc. / Home / Ccs view the non-flash version of this site
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| Page title: | Certified Compliance Solutions, Inc. / Home / Ccs |
| Keywords: | Certified Compliance, Certified Compliance Solutions, Certified Software, Certified Software Solutions, CCS, CSS, FDA, FDA Compliance, FDA Regulatory Compliance, FDA QSR, FDA QSR 820, FDA QSR 820.30, QSR Compliance, Regulatory Compliance, Quality System, Quality System Audits, Quality System Implementation, QSR, V&V, 510(k), PMA, Verification, Validation, Verification & Validation, Medical Device, Medical Device Manufacturer, Manufacturing Process Validation, Medical Device Regulation, Medical Device Reporting, Medical Device Software, Medical Device SW, MDR, Part 11, Part 11 Compliance, Process Validation, Software Validation, 483, FDA Warning Letter, Regulatory Submissions, Pre-Market Approval, De-Novo, Human Factors in Engineering, Usability Engineering, Usability Testing, Usability, ISO 13485, ISO 14971, IEC 62304, IEC 62366, GPSV, Software life cycle processes, SDLC, Software Development Lifecycle, Quality, Quality Assurance, Quality Engineering, Dan Olivier, Daniel Olivier, Daniel P. Olivier, Chris Olivier, Chris J. Olivier, Tom Bento, Thomas Bento, Al Pacheco, Brian Weller, IEC 60601-1, Medical device directive, MDD, IVDD, Medical equipment, Medical electrical equipment, Safety & effectiveness, Substantial equivalence, Substantially equivalent, FDA Clearance, FDA Compliance, FDA Compliant, FDA Guidance, FDA Inspection, FDA Audit, Quality System Implementation, Quality System Audit, Safety Risk, Safety Risk Management, Safety Risk Analysis, Software Requirements, Software Requirements Specification, System Requirements Specification, Requirements Traceability, Traceabiltity Matrix, Software Design Description, System Design Description, Safety Architecture, Safety Requirements, Software Validation Plan, System Validation Plan, Software Validation Test, System Validation Test, Software Validation Protocol, System Validation Protocol, Validation Summary Report, Unit Testing, Integration Testing, Software Code Review, SW Development, Software Development, Software Validation, FDA Regulatory Compliance, Risk Control Measures, RCM, Safety Mitigation, Broadly Acceptable Region, As Low As Reasonably Practicable, ALARP, Hazard Analysis, 21 CFR 820, 21 CFR 820.30, 21 CFR Part 11. |
| Description: | Medical Device & Pharmaceutical Regulatory Compliance Expert Consultants specializing in assuring compliance with FDA regulations & ISO standards. |
| IP-address: | 216.70.101.92 |
WHOIS Info
| NS | Name Server: NS23.DOMAINCONTROL.COM Name Server: NS24.DOMAINCONTROL.COM |
| WHOIS | Status: clientDeleteProhibited Status: clientRenewProhibited Status: clientTransferProhibited Status: clientUpdateProhibited |
| Date | Creation Date: 27-dec-2006 Expiration Date: 27-dec-2018 |