Octave Reliance Lab Investigation
Formerly ETQ Reliance Lab Investigation.
Manage lab investigation with consistency and ease with OOS software
Future-proof your quality investigations
Establishing a dedicated process streamlines triage, investigation and problem-solving. Out-of-spec software creates a standardized process that ensures every investigation is conducted consistently, promptly and with the correct steps taken in the right order. Lab Investigation from Reliance OOS software efficiently tracks, trends and resolves problems identified in laboratory testing.
A systematic approach to lab investigations
Reliance OOS software helps document the investigation process of an out-of-specification or out-of-trend lab test result. Users now have the ability to investigate a result to determine the cause and conduct re-sampling or re-testing to confirm results. Interconnected OOS software was designed for any industry that tests products in a laboratory. Unexpected lab results require further investigation.
Document out-of-specification and out-of-trend results
Document the investigation process for any out-of-specification or out-of-trend lab test result. Users can investigate results to determine the cause and conduct re-sampling or re-testing to confirm test results through a standardized investigation process.
Investigate root causes of OOS and OOT results
OOS Investigation software can help determine risk. A user can generate a corrective action or Nonconformance material report after determining if one is required. In many cases, OOS Investigation can eliminate the need for a more costly CAPA process.
Directly initiate CAPA or NCMR from Lab Investigation
The interconnected OOS software was designed for any industry that tests products in a laboratory, not just life science customers. Unexpected lab results require further investigation. The integrated Lab Investigation software streamlines that process.
Efficiently track, trend and resolve lab investigation results
The interconnected OOS software was designed forany industry that tests products in a laboratory. Unexpected lab results require further investigation. The integrated Lab Investigation software streamlines that process.
Maintain compliance with pharmaceutical and life sciences regulations
For organizations that must comply with cGMP and 21 CFR Part 210 and 211 requirements such as pharmaceutical and combination product makers, Lab Investigation from Reliance OOS software enables you to capture and track your processes and results for complete compliance.
Standardize lab investigation processes across your organization
An out-of-spec software plays a key role by creating a standardized process that ensures every investigation is conducted consistently, promptly and with the correct steps taken in the right order. This standard approach helps future-proof your organization against potential issues.
Measurable returns across quality operations
Organizations across industries have successfully implemented Reliance to manage their lab investigations and quality events. These results demonstrate the impact of a systematic, standardized approach to OOS and OOT investigations. By establishing dedicated processes for lab investigation, companies reduce risk, maintain compliance and resolve quality issues faster.
0%
50%reduction in CAPA resolution time
0%
40%reduction in document revision time
0%
45%Reduction in audit findings
Results based on case studies from leading pharmaceutical, life sciences and manufacturing organizations. Statistics reflect improvements achieved through implementation of standardized lab investigation processes and quality event management systems. Individual results may vary based on implementation approach, organizational factors, industry requirements and specific use cases.
Client success stories
Reliance was selected because it was flexible, highly configurable, easy to modify in house — and it was FDA and EU compliant, giving audit trail electronic signatures traceability.
Reliance was selected because it was flexible, highly configurable, easy to modify in house — and it was FDA and EU compliant, giving audit trail electronic signatures traceability.
Resources to sharpen your quality strategy
From decision frameworks to implementation checklists, we've compiled the insights quality leaders need to drive results. These practical guides help you build business cases, navigate compliance requirements and accelerate your quality transformation.
We're here to help
Get the help you need with direct access to support and resources.
