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21 CFR Part 58 - Good Laboratory Practice (GLP) for Compliance Officers

What does 21 CFR Part 58 - Good Laboratory Practice (GLP) require of a Compliance Officer?

Title 21 Code of Federal Regulations Part 58 establishes Good Laboratory Practice (GLP) regulations for nonclinical laboratory studies supporting applications for research or marketing permits for FDA-regulated products. Under 21 CFR Part 58 - Good Laboratory Practice (GLP), which defines 25 controls, a Compliance Officer's work is deciding which controls you own outright, which you share and which belong to another team, then holding the evidence for the first group.

Which 21 CFR Part 58 - Good Laboratory Practice (GLP) controls land on the Compliance Officer

Compliance Officers ensure the organisation meets its regulatory obligations. They manage audit programmes, maintain evidence repositories, track regulatory changes, and coordinate across business units to sustain compliance posture.

21 CFR Part 58 - Good Laboratory Practice (GLP) defines 25 controls across 7 domains that directly affect the Compliance Officer role. Understanding which controls fall within your ownership, which are shared, and which are owned by other teams is the foundation of effective compliance management.

What a Compliance Officer is accountable for under 21 CFR Part 58 - Good Laboratory Practice (GLP)

1

Monitoring regulatory changes and assessing their impact on the organisation

2

Managing internal and external audit programmes and evidence collection

3

Maintaining compliance documentation, policies, and control frameworks

4

Coordinating with business units to implement and maintain required controls

5

Reporting compliance status to senior leadership and regulatory bodies

Where Compliance Officers lose time on 21 CFR Part 58 - Good Laboratory Practice (GLP)

These are the most common obstacles Compliance Officers face when managing 21 CFR Part 58 - Good Laboratory Practice (GLP) compliance, and how to address them:

Challenge 1

Tracking overlapping requirements across multiple regulatory frameworks

Challenge 2

Collecting evidence from multiple teams and systems for audit readiness

Challenge 3

Keeping policies and procedures current as regulations change

Challenge 4

Demonstrating compliance ROI to justify programme investment

Challenge 5

Managing the volume of regulatory change across jurisdictions

A working order for a Compliance Officer starting on 21 CFR Part 58 - Good Laboratory Practice (GLP)

1. Readiness Assessment

Take a 5-minute readiness assessment to identify your organisation's current gap profile against 21 CFR Part 58 - Good Laboratory Practice (GLP). Get a prioritised action plan tailored to your specific situation.

2. Cross-Framework Mapping

Use our platform to map 21 CFR Part 58 - Good Laboratory Practice (GLP) controls against other frameworks you already comply with. 21 CFR Part 58 - Good Laboratory Practice (GLP) maps to 182 other frameworks in our database.

3. Build Your Toolkit

Equip yourself with 21 CFR Part 58 - Good Laboratory Practice (GLP) toolkits, self-assessments, and implementation guides from our store. Resources designed specifically for Compliance Officers managing compliance programmes.

4. Continuous Monitoring

Establish ongoing compliance monitoring using our platform's gap analysis tools. Track your maturity over time and demonstrate progress to stakeholders.

21 CFR Part 58 - Good Laboratory Practice (GLP) in your sector

21 CFR Part 58 - Good Laboratory Practice (GLP) for Healthcare→21 CFR Part 58 - Good Laboratory Practice (GLP) for Financial Services→21 CFR Part 58 - Good Laboratory Practice (GLP) for Technology→21 CFR Part 58 - Good Laboratory Practice (GLP) for Government→21 CFR Part 58 - Good Laboratory Practice (GLP) for Manufacturing→21 CFR Part 58 - Good Laboratory Practice (GLP) for Energy→21 CFR Part 58 - Good Laboratory Practice (GLP) for Retail→21 CFR Part 58 - Good Laboratory Practice (GLP) for Education→

Who else owns part of 21 CFR Part 58 - Good Laboratory Practice (GLP)

21 CFR Part 58 - Good Laboratory Practice (GLP) for CISOsView guide →21 CFR Part 58 - Good Laboratory Practice (GLP) for Risk ManagersView guide →21 CFR Part 58 - Good Laboratory Practice (GLP) for IT DirectorsView guide →21 CFR Part 58 - Good Laboratory Practice (GLP) for DPOsView guide →21 CFR Part 58 - Good Laboratory Practice (GLP) for AuditorsView guide →

Questions Compliance Officers ask about 21 CFR Part 58 - Good Laboratory Practice (GLP)

What does a Compliance Officer need to know about 21 CFR Part 58 - Good Laboratory Practice (GLP)?
As a Compliance Officer, your key responsibilities under 21 CFR Part 58 - Good Laboratory Practice (GLP) include monitoring regulatory changes and assessing their impact on the organisation and managing internal and external audit programmes and evidence collection. The framework contains 25 controls that fall within your area of responsibility. Understanding which controls you own versus which are shared with other teams is critical for effective implementation.
How does 21 CFR Part 58 - Good Laboratory Practice (GLP) affect the Compliance Officer role?
21 CFR Part 58 - Good Laboratory Practice (GLP) directly impacts Compliance Officers through monitoring regulatory changes and assessing their impact on the organisation, managing internal and external audit programmes and evidence collection, maintaining compliance documentation, policies, and control frameworks. The framework provides structure that helps Compliance Officers demonstrate due diligence and report compliance status to stakeholders.
What are the biggest 21 CFR Part 58 - Good Laboratory Practice (GLP) challenges for Compliance Officers?
Common challenges include tracking overlapping requirements across multiple regulatory frameworks; collecting evidence from multiple teams and systems for audit readiness; keeping policies and procedures current as regulations change. Using cross-framework mapping tools and automated evidence collection can significantly reduce these pain points.
How should a Compliance Officer prepare for a 21 CFR Part 58 - Good Laboratory Practice (GLP) audit?
Start by conducting a readiness assessment to identify gaps. Then focus on maintaining compliance documentation, policies, and control frameworks and coordinating with business units to implement and maintain required controls. Maintain a current evidence repository and ensure all control owners have documented their processes. Our readiness reports provide a prioritised action plan specific to your gap profile.
What tools help Compliance Officers manage 21 CFR Part 58 - Good Laboratory Practice (GLP) compliance?
Effective 21 CFR Part 58 - Good Laboratory Practice (GLP) compliance management requires tools for gap analysis, control mapping, evidence collection, and reporting. Our compliance platform provides AI-powered gap analysis across 1,121 frameworks with 315K+ verified control-to-control mappings, helping Compliance Officers identify overlapping requirements and reduce duplicate compliance effort.

Compliance Officer: How ready is your organisation for 21 CFR Part 58 - Good Laboratory Practice (GLP)?

Answer 25 questions and get a professional readiness report with gap analysis, maturity scores, and prioritised action items. Results in 5 minutes.

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Written and maintained by Gerard Blokdyk, The Art of Service.Last updated .