Residue Chemistry & Bioanalytical Services
At Symbiotic Research, management and employees have combined over 100 years of experience in conducting residue chemistry/bioanalytical studies.
Our team is highly adept in residue chemistry related registration issues hence we offer better risk management when coordinating animal, poultry, crustacean and fish residue studies, designing residue storage stability, residue method development/validation and residue analysis to help curb future registration dilemma. Our team/principal investigators and/or study directors have a long history of working directly with various animal research facilities specially our own subsidiary-Genesis Midwest. Our study directors are highly skilled in coordinating sample shipments to analytical labs, sample process, stability study setup, method development or adaptation, method validation and GLP residue sample analysis.
GLP compliant laboratory
Symbiotic Research bioanalytical lab is fully GLP compliant and meets FDA and EPA requirements for data acceptance. Our bioanalytical lab equipped with the latest in triple quads such as AB SCIEX 5500, 4000 and the latest in high resolution quantitation technique-MRM-HR utilizing AB SCIEX X500B. Our sample runs created through WATSON LIMS DATA MANAGEMENT SYSTEM 7.6.1 SP1 and uploaded either to Analyst or Sciex’s latest OS-based software and reviewed by WATSON LIMS DATA MANAGEMENT system.
Quality Assurance
Our instruments go through annual OQ/PV validation procedures and all data generated are real-time backed up into three different locations: local drive, local server and the cloud.
Animal residue and bioanalytical chemistry
Our team is specialized in animal, poultry, fish, crustacean, companion animal residue chemistry.
Analytical methods
From science-based concepts to adaptation or development of methodology to validation of methods, we offer all the necessary steps in creating robust, proven, and exact analytical methods:
- Methods for active ingredient(s) and formulated product
- Certificate of analysis
- Development and validation of single & multi-residue analysis methods
- Identification and optimization of sample preparation (including solid-phase extraction, QuEChERS, etc.)
- Enforcement methods & radio-validation of analytical methods
- Screening: purity & impurity profile of the active substance
- 5‑Batch analyses