Recommended

EU-India conclude Free Trade Agreement
Pennsylvania to home Lilly fourth new US manufacturing facility
WEBINAR | Harnessing AI for more efficient clinical trials | REGISTER TODAY
Increasing the effectiveness of pharma endotoxin testing | REGISTER NOW
WEBINAR | Practical considerations for aseptic gowning in contamination control strategies
AstraZeneca commits $15bn to Chinese manufacturing
Roche GLP-1 promising in phase II obesity trial
WuXi Biologics and HanchorBio collaborate on next-gen immunotherapies
Innovative nanoparticle research potential AMR breakthrough
Harnessing digital PCR for rapid sterility testing | WEBINAR
Realising autonomous pharmaceutical operations – register now
Explore the latest issue here
Complying with USP Chapters 41 and 1251 revisions for pharma quality control | WEBINAR
webinar

ISO/IEC 17025:2017 – New definitions for specifications, decision rules & risk assessments for calibrations

Supported by:

5 June 2018

11
SHARES

Supported by:

5 June 2018

ABOUT THIS WEBINAR:

The 2017 revision to ISO/IEC 17025 includes better guidance on conformity and a new risk-based approach. In this webinar we discuss the revision in terms of temperature and humidity calibration in life science environments. In this webinar you will learn:

 

SECURE YOUR FREE SPOT

 


This webinar to explore rapid sterility testing methods that ensure fast, reliable product release, addressing critical challenges in timely delivery and safety.

Harnessing digital PCR for rapid sterility testing | 18 March 2026 | 3PM

What you’ll discover:

  • Rapid sterility testing methods that address the challenge of lengthy testing times, improving efficiency and ensuring timely product release
  • Insights into how digital PCR technology enhances testing accuracy and sensitivity, detecting contaminants quickly and reliably
  • Real-world case studies on rapid testing implementations in the field of cell and gene therapy

A Q&A session at the end of the webinar gives the audience a chance to ask questions, such as how to implement these technologies effectively.

Register now – it’s free

  • How to decide if ISO 17025 is a requirement for your application, or if ISO 9001 calibration is sufficient.
  • How to deal with the revision’s new requirement for clear definitions for specifications and decision rules.
  • How to use risk assessment as a tool to decide which standard to follow for calibrations in regulated environments.

KEYNOTE SPEAKERS:

Paul Daniel Paul Daniel – Senior Regulatory Expert, Vaisala

Paul Daniel is the Senior Regulatory Compliance Expert at Vaisala. He oversees and guides the validation program for the Vaisala viewLinc environmental monitoring system. Paul also shares his GMP experience through regular blog contributions, webinars, and seminars around the world. He serves as a customer advocate to ensure the viewLinc environmental monitoring system matches the demanding requirements of life science and regulated applications.

Daniel Soave – Technical Support Service Manager, Vaisala

Daniel Soave is a Process Quality Engineer and has been a Quality Manager for Vaisala. He is currently the Technical Support Manager for Vaisala’s continuous monitoring product in North America. Daniel is also responsible for developing, maintaining and improving the quality management systems in Vaisala’s Boston calibration lab, with special focus on ISO9001, ISO14001, OHSAS18001 and ISO17025.

Jennifer Clay – Calibration Service Manager, Vaisala

Jennifer Clay has ten years of experience doing meteorological metrology at Vaisala’s ISO 17025 accredited calibration lab in Boston, US.

 

 
Share via
Share via