Testifying at FDA’s First Public Hearing on Cannabis Extract
Last week, Matthew Sica, Accreditation Manager, RMP, PT, and Medical, testified at the U.S. Food and Drug Administration’s first public hearing on how to regulate […]
AuthorMatthew Sica, Accreditation Manager, RMP, PT, and Medical
Is Your CBD Oil Safe?
The 2019 Farm Bill approved by Congress in December 2018 allows hemp cultivation broadly, reversing previous restrictions. But just because hemp products are more available, […]
Impact of the ISO/IEC 17025:2017 Transition, Part 6
This is the final post about the transition to ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories. To recap, our first […]
Impact of the ISO/IEC 17025:2017 Transition, Part 5
This is the fifth in a series of posts about the transition to ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories. […]
Impact of the ISO/IEC 17025:2017 Transition, Part 4
This the fourth post about the transition to ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories, the global standard for calibration […]
Impact of the ISO/IEC 17025:2017 Transition, Part 3
This is our third post about the transition to ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories, the global reference for […]
Impact of the ISO/IEC 17025:2017 Transition, Part 2
This is the second in a series of posts about ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories, the global reference […]
ISO/IEC 17025:2017 Transition: Impact on Labs and Customers (Part 1)
This is the first in a series of posts about the recently published ISO/IEC 17025:2017, General requirements for the competence of testing and calibration laboratories, […]