Скачать или смотреть Six Steps to Effective Temperature Mapping

Free Webinar to Simplify Compliance and Strengthen Audit Readiness

Are you confident in your temperature mapping process?

For professionals in pharmaceutical, biotech, and laboratory environments, temperature mapping is more than a regulatory requirement—it's a foundational element of product quality, patient safety, and audit readiness.

Despite its critical role, many teams still encounter common pitfalls: improper sensor placement, incomplete documentation, and non-compliant protocols that fail under regulatory scrutiny.

Why This Webinar Matters

Temperature mapping is mandated by regulatory bodies including the FDA, EMA, WHO, and under EU GDP requirements. These standards continue to evolve, placing increased pressure on teams to demonstrate robust, repeatable, and compliant mapping practices.

Improper execution can result in:

Missed critical hot or cold spots
Delays in product release or regulatory approval
Risk of non-compliance during inspections
Compromised sample integrity or product loss
This webinar offers a proven framework to help you avoid these issues—drawing from over two decades of real-world validation experience.

What You Will Learn

Join me, Nathan Roman, Director at Ellab and author of Six Steps to Effective Temperature Mapping, as I walk through my step-by-step framework designed to reduce mapping errors and increase inspection confidence:

1. Understanding the Foundations

Learn the regulatory drivers behind temperature mapping and the consequences of falling short.

2. Prerequisite Documentation

Establish a solid foundation with SOPs, risk assessments, and project plans that ensure alignment and success.

3. User Requirement Specifications (URS)

Create meaningful URS documents that reflect operational needs and stand up to auditor review.

4. Walkdown Execution

Conduct proper walkdowns to identify risks in airflow, loading patterns, and mechanical integrity before testing begins.

5. Sensor Placement Strategy

Move beyond standard grid methods—place sensors to capture worst-case scenarios and ensure meaningful data analysis.

6. Audit-Ready Protocols and Reporting

Design protocols and reports that meet compliance expectations, including Annex 15, 21 CFR Part 11, and data integrity requirements.

Who Should Watch

This webinar is tailored for:

Validation and QA professionals preparing for regulatory inspections
Lab and facility managers responsible for controlled temperature units, including freezers, incubators, and warehouses
Operations and compliance leaders addressing recurring mapping challenges or implementing new systems

Why You Should Watch

Attendees will gain:

Practical tools to improve temperature mapping accuracy and consistency
Insights from pharmaceutical and biotech case studies
Time-saving tips that support ongoing compliance and audit readiness
A live Q&A session to address specific challenges and scenarios

Final Thoughts

Temperature mapping should never be an afterthought—it is a critical component of your overall qualification and compliance strategy. This webinar offers a chance to elevate your process, eliminate guesswork, and ensure every study meets the highest standards of data integrity and regulatory compliance.