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Beyond the Checklist
Performance Validation
5 episodes
1 month ago
“Beyond the Checklist” is a podcast that explores not only the essential aspects of cGMP but also explores the human factors that drive excellence in life sciences manufacturing. Through expert interviews, industry insights and real-world discussions, we uncover how culture, leadership and innovation shape a safer, more efficient path to market. Join us as we navigate the complexities of regulatory requirements while highlighting the people and processes that elevate compliance from a box-checking exercise to a mindset of continuous improvement. In the highly regulated world of pharmaceutical, medical device and biotechnology manufacturing, compliance is critical — but true quality goes beyond the checklist.
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Science
Business,
Management
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All content for Beyond the Checklist is the property of Performance Validation and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
“Beyond the Checklist” is a podcast that explores not only the essential aspects of cGMP but also explores the human factors that drive excellence in life sciences manufacturing. Through expert interviews, industry insights and real-world discussions, we uncover how culture, leadership and innovation shape a safer, more efficient path to market. Join us as we navigate the complexities of regulatory requirements while highlighting the people and processes that elevate compliance from a box-checking exercise to a mindset of continuous improvement. In the highly regulated world of pharmaceutical, medical device and biotechnology manufacturing, compliance is critical — but true quality goes beyond the checklist.
Show more...
Science
Business,
Management
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What They Don’t Teach You About Temperature Mapping: Real Talk With Validation Expert Paul Daniel
Beyond the Checklist
36 minutes 19 seconds
6 months ago
What They Don’t Teach You About Temperature Mapping: Real Talk With Validation Expert Paul Daniel

In this episode, we’re joined by Paul Daniel, Senior GxP Regulatory Expert of Vaisala, who brings nearly 30 years of experience in pharmaceutical validation and temperature mapping. Paul shares the evolution of mapping from a technical task to a regulatory imperative, unpacking the misconceptions, equipment considerations and quality frameworks essential for accurate, compliant execution.



Key Takeaways:


(04:19) Modern data loggers reduce manual steps and lower mapping error rates.

(07:00) New mapping guidance added complexity and confusion to established practices.

(10:22) Mapping provides documented evidence your CTU operates in a controlled state.

(12:33) Misunderstanding mapping as simple logging indicates the lack of a validation framework.

(15:05) Superior equipment improves data quality and helps navigate inevitable deviations.

(23:26) If you don’t understand the tools, it’s time to outsource.

(26:28) Warehouse automation can streamline mapping with robotic logger placement.

(33:50) Deviations expose real-world system behavior and improve validation expertise.


Resources Mentioned:


Paul Daniel

https://www.linkedin.com/in/paul-daniel-37176518/


Vaisala | LinkedIn

https://www.linkedin.com/company/vaisala


Vaisala | Website

https://www.vaisala.com/en




Thank you for listening to “Beyond the Checklist.” Be sure to leave us a review and subscribe so you don’t miss any episodes. 


For more information, visit www.perfval.com. 




#cGMPCompliance #FDARegulations #QualityAssurance #CQV

Beyond the Checklist
“Beyond the Checklist” is a podcast that explores not only the essential aspects of cGMP but also explores the human factors that drive excellence in life sciences manufacturing. Through expert interviews, industry insights and real-world discussions, we uncover how culture, leadership and innovation shape a safer, more efficient path to market. Join us as we navigate the complexities of regulatory requirements while highlighting the people and processes that elevate compliance from a box-checking exercise to a mindset of continuous improvement. In the highly regulated world of pharmaceutical, medical device and biotechnology manufacturing, compliance is critical — but true quality goes beyond the checklist.