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Welcome to C-Path Software Engineering. Expertise in high integrity software. Project Planning and Management. Verification and Validation,. Quality Management and Assurance. Documentation and Technical Writing. C-Path provides specialist consultancy services to the medical device sector. And has extensive knowledge and experience in the regulatory approvals processes for software and the expected quality procedures, standards and documentation. Send mail to info@cpathse.co.uk.

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Welcome to C-Path Software Engineering. Expertise in high integrity software. Project Planning and Management. Verification and Validation,. Quality Management and Assurance. Documentation and Technical Writing. C-Path provides specialist consultancy services to the medical device sector. And has extensive knowledge and experience in the regulatory approvals processes for software and the expected quality procedures, standards and documentation. Send mail to info@cpathse.co.uk.
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Home | cpathse.com Reviews

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Welcome to C-Path Software Engineering. Expertise in high integrity software. Project Planning and Management. Verification and Validation,. Quality Management and Assurance. Documentation and Technical Writing. C-Path provides specialist consultancy services to the medical device sector. And has extensive knowledge and experience in the regulatory approvals processes for software and the expected quality procedures, standards and documentation. Send mail to info@cpathse.co.uk.

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cpathse.com cpathse.com
1

Development

http://www.cpathse.com/Development.htm

Professional development of a commercial software product should be performed using a structured process which addresses software life cycle management, risk management, software engineering, verification and validation and all supporting documentation. C-Path employs a structured risk-based approach to software development using design control processes to produce quality solutions and appropriately verified and validated software for: real-time embedded systems, desktop applications and hybrid systems.

2

Medical Devices

http://www.cpathse.com/medicaldevices.htm

Software targeted for the medical device market, requires adherence to stringent regulatory and quality standards. C-Path have experience in taking a number of medical software products of varying levels of concern from concept to market. We offer a complete support service for medical software development and in addition to design and coding, we can assist in:. Planning, implementation and documentation of Risk Management. Generation of Technical Files/Dossiers. Generation of Design History Files.

3

Regulatory & Quality Compliance

http://www.cpathse.com/Regulatory.htm

Quality and Regulatory Compliance. Good software engineering practice includes effective quality assurance integrated into any software development project. A formal means of controlling documents, maintaining records, reporting incidents and verifying important processes, (including software development and quality processes), supports regulatory compliance requirements in all regions of the world. Standards, practices and conventions. Problem reporting and corrective action. C-Path Software Engineering...

4

Re-Engineering

http://www.cpathse.com/Reengineer.htm

Legacy software that resides in (i) systems that have yet to be commercialized or (ii) in established commercial products can often be a challenge to manufacturers when software development (or maintenance) is required and driven by system anomalies, component. Bsolescence, regulatory or market needs. Often little or no documentation exists for the legacy software, the architecture and design may be outdated or obsolete and the original developers may no longer be available. Iii) Code reviews and analysis.

5

Documentation

http://www.cpathse.com/Documentation.htm

Documentation and Technical Writing. A well documented software product contributes to the overall quality and robustness of the target system, provides transparency and reduces maintenance costs. Documentation, however, can be a laborious tasks and typically the effort required to appropriately document a software product is often underestimated. C-Path can help alleviate the documentation effort, freeing up resources to concentrate on application development. Send mail to info@cpathse.co.uk.

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Welcome to C-Path Software Engineering. Expertise in high integrity software. Project Planning and Management. Verification and Validation,. Quality Management and Assurance. Documentation and Technical Writing. C-Path provides specialist consultancy services to the medical device sector. And has extensive knowledge and experience in the regulatory approvals processes for software and the expected quality procedures, standards and documentation. Send mail to info@cpathse.co.uk.

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