Quality Systems in Metabolomics: Internal Standards & Suitability — Hands-on

Learn how to embed robust quality systems into metabolomics workflows. You will design internal standard strategies, plan QC and system suitability checks, understand key method validation elements and build traceable, audit ready documentation that supports both research and regulated applications.

Quality Systems in Metabolomics: Internal Standards & Suitability

Help Desk · WhatsApp

Session Index

Session 1 — Quality Systems & Regulatory Expectations Session 2 — Internal Standards Strategy & Implementation Session 3 — System Suitability, QC Samples & Monitoring Session 4 — Documentation, Audits & Continuous Improvement

Session 1

Fee: Rs 8800

Quality Systems & Regulatory Expectations

Quality systems language for metabolomics labs

fit for purpose method thinking accuracy, precision and robustness concepts traceability and chain of custody basics

Regulatory and guideline landscape touch points

GLP and ISO style expectations bioanalytical validation guidance ideas journal and consortium recommendations

Where quality systems sit in the metabolomics pipeline

study design and sample handling acquisition and processing checks reporting and data retention

Session 2

Fee: Rs 11800

Internal Standards Strategy & Implementation

Roles of internal standards in metabolomics and lipidomics

monitoring extraction and injection variability normalising instrument response supporting semi quantitative reporting

Selecting and grouping internal standards

class matched and isotopically labelled options spike levels and linear range considerations panel design for broad coverage

Practical implementation and tracking of internal standards

spike timing and mixing order monitoring recovery and drift across runs flagging problematic batches or samples

Session 3

Fee: Rs 14800

System Suitability, QC Samples & Monitoring

System suitability checks before and during runs

retention time and peak shape criteria background and carryover checks sensitivity and SNR thresholds

QC sample design and placement in metabolomics runs

pooled QC concepts and preparation injection frequency and run order patterns RSD style feature filtering using QC

Monitoring performance over time and across studies

control charts for key metrics trend detection and intervention rules documenting issues and corrective actions

Session 4

Fee: Rs 18800

Documentation, Audits & Continuous Improvement

Core documentation set for metabolomics quality systems

SOPs and work instructions logbooks and electronic records processing manifests and data dictionaries

Audit trails, deviations and corrective actions

capturing deviations and impact assessment root cause style thinking CAPA documentation basics

Continuous improvement and readiness for collaboration or audits

periodic review of QC metrics and SOPs checklists for external partners or reviewers building a culture of quality in metabolomics teams

PDF

Quality Systems in Metabolomics: Internal Standards & Suitability Training | QC, System Suitability & Compliance

Quality Systems in Metabolomics: Internal Standards & Suitability — Hands-on