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Are you looking for ways to increase your compliance effectiveness? Complex and extensive federal regulations demand a systematic approach to document creation, review, approval and security throughout the drug development and manufacturing process. IBM Regulatory Content Services for Life Sciences can help your company manage its development and manufacturing to meet federal regulations by supplying you with a foundation for managing compliant content, while providing faster implementation and accelerated time to generate revenue. Our services help ensure that all documents are available and appropriate, increasing your compliance effectiveness.
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GXPharma Documentum product suite
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- Quick extraction of data.
- Control access to data.
- Increased value of existing databases.
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System–controlled support for electronic records
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- Manages content in compliance with the FDA's prescribed regulatory requirements.
- Standardized, consistent formats.
- Allows for quick review of data.
- Adaptability to evolving regulatory requirements.
- Potential for accelerated time to market.
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Documentum DocControl manager
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- Capability to configure documents to comply with Good Manufacturing Practices.
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IBM TotalStorage® solutions
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- Disaster–tolerant storage for scientific and technical computing.
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IBM eServer xSeries® systems
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- Scalable and easy to cluster.
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