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Regulatory Affairs
Regulatory Affairs (RA) is a profession that ensures compliance within industries such as: pharmaceuticals, energy production, banking, and agrochemicals. RA works with government on all levels in order to monitor and advise on laws that coincide with a business. Such partnerships include: Food and Drug Administration, Securities and and Exchange Commission, and the Department of Energy.
FEB 24, 2021 | 12:00 AM
There are approximately 2000 distinct lipids which are believed to influence health and disease in humans. Their molecular interplay with genes, proteins and metabolites is strongly affected...
DEC 11, 2020 | 7:00 AM
Date: November 16, 2020 Time: 7:00am (PST), 10:00am (EST) Join us for a webinar to learn about quality control (QC) regulations, setting the proper QC strategy/design, and troubleshoot SARs...
NOV 12, 2020 | 9:00 AM
Testing volumes need to increase by orders of magnitude in order to restore communities back to normality. This workshop focuses on solutions that equip laboratories to participate in expand...
OCT 28, 2020 | 6:00 AM
DATE: October 28, 2020 TIME: 6:00am PST Tumorigenesis and cancer progression are affected by the tumor immune microenvironment (TIME). The TIME not only influences the efficiency of existing...
OCT 20, 2020 | 5:00 AM
Date: October 20, 2020 Time: 5:00am (PDT), 8:00am (EDT), 2:00pm (CEST) With the COVID-19 pandemic as one of the biggest challenges to our modern world, Bruker has taken an active part suppor...
OCT 13, 2020 | 5:00 AM
Date: October 13, 2020 Time: 5:00am (PDT), 8:00am (EDT) Dr. Markus Kostrzewa shall ellaborate the progress that has been made in Bruker Microbiology Research and Development, including new p...
JUL 30, 2019 | 6:00 AM
DATE: July 30, 2019TIME: 6:00am PT, 9:00am ET The current version of the EMA Guideline for the environmental risk assessment of human drugs was published in 2006. This guidance...
MAR 28, 2019 | 6:00 AM
The vast majority of US states and other countries require quality control testing of cannabis and cannabis processed products prior to release for distribution. The purpose of product...
MAR 27, 2019 | 6:00 AM
There are currently 33 states and the District of Columbia that have legalized medical marijuana. The research supporting its medical use, however, lags behind current policy efforts. This ta...
FEB 13, 2019 | 10:30 AM
Xenobiotic-induced cardiotoxicity is a major concern for both pharmaceuticals and chemicals in the marketplace. For drugs, "Thorough QT/corrected QT (QTc)" (TQT) studies are corners...
OCT 09, 2018 | 8:00 AM
DATE: October 9, 2018TIME: 08:00am PDT, 11:00pm EDT Have you ever wondered what to consider when you are selecting ancillary materials for your cell therapy clinical research...
FEB 09, 2017 | 3:00 PM
DATE: February 9, 2017TIME: 3:00pm PT, 6:00pm ETThe presentation will very briefly cover the regulatory system for lab animals in China, as well as the regulations and guidelines a...
NOV 17, 2016 | 9:00 AM
This panel will discuss quality requirements of ancillary materials used in cell therapy manufacturing, relevant standards and how requirements vary by phase. Participants will learn wh...
