Remote Work - Data Review using TeamViewer or Remote Desktop Programming - Safe Distancing during COVID-19.
Research and Development - Sample Preparation, Methods and Formulations Development/Testing.
QMS Systems- Qualtrax and MC Analyze.
Onsite GAP Assessments (Audit Laboratory Methods, SOPs, Staffing-Training and Competency)
Clinical Toxicology
Document development of ISO 17025 Policy and Procedures
Partnership with ISO 17025 Accreditation Agencies to Ensure Audit Readiness - A2LA, ANAB, PJ
Regulatory—FDA, CLIA, DEA, GMP, GLP, ISO 17025-2017
Lab Accreditation: COLA, CAP
Quality Management Systems Design and Remediation including Deviations, Non-Conformities, OOS, and CAPA
Quality Manual Design
Change Management
SOP Development and Documentation Review
Labor Analysis and Benchmarking
Review of State Regulatory Requirements
Equipment Recommendations to Meet State Testing Action Limits and Requirements
Technical Procedures
Methods Development, Validation, and Optimization (rapid and cost effective)
Facility Planning - Laboratory Design and Build-Out, including Capital Equipment Evaluation
Streamlining of Existing Methods (HPLC, LCMSMS, GC, GCMS)
Identity and Quantification of Components of Complex Formulations
Operations Assessment and Enhancement - Workflow Analysis
Core Laboratory Analysis/Development
Personnel Training and Education
Interim Laboratory Management/Director
Cost Analysis (testing samples)
Business Plan Preparation
Technical Writing and Presentations
Scientific Expert Witness Services