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| Safety Pharmacology and Toxicology |
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DISS CA Recorder/VR2 are routinely used in the GLP-regulated safety pharmacology environment. We are a recognized leader of GLP-compliant data acquisition, analysis, and management systems.
- Validated by major pharmaceutical companies and contract research organizations
- Meets 21 CFR, Part 11 user requirements throughout the system
- Proven quality management system with Software Development Life Cycle
- Complete IQ documentation of your system from assembly to post-installation
- Meets data analysis requirements for ICHS7A guidelines for cardiovascular, respiratory, neurological, and GLP studies
- Onsite training and validation support with complete SOPs and certificates
- Validation Help Book with list of SOPs for your in-house validation
- Yearly re-validation services
- Optional customized network security configuration can be provided during on-site installation
>> Ask for a quote
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"I have used CA Recorder for several years and consider it to be the highest quality, most accurate and best-supported data acquisition system available for pharmacological research." |
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