Complying with an ISO procedure requires a lot more than following the instructions in an ISO procedure manual. Doing it right requires the technology for streamlining ISO processes. This is the only way to really comply with an ISO procedure or ISO standard. It is also the only way to keep pace with customer and patient expectations for high quality products.
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Each ISO procedure or ISO standard provides detailed information about quality requirements in a specific area. Examples of standards that you are probably familiar with include ISO 9001 2000 and other standards related to ISO 9000 (quality management), ISO 14000 (environmental management), and ISO 13485 quality systems for medical device manufacturers). Additional ISO standards include the following:
MasterControl can help your company comply with an any ISO procedure or standard. We provide process management, document control, and risk-based validation solutions. We also provide a variety of services that comply with both FDA and ISO standards. With MasterControl, you don't have to worry about complying with a ISO procedure (whether it be ISO 9001 2000, ISO 14971 or ISO 13485 -- or any other ISO procedure).
That's because, at MasterControl, we automate compliance. This translates into you not having to worry about maintaining documents or managing audit trails. We automate everything having to do with an ISO procedure, including document approval routes, deviations, CAPA, change control, training, etc. And, best of all, we do it using one web-based/integrated platform.
To learn about how MasterControl, a provider of quality management and document control software, can help life science and general manufacturers streamline quality, ISO procedure compliance and document control. Please feel free to contact a MasterControl representative.
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