Pharmaceutical water is the most used ingredient in pharmaceutical industries being used directly for the drug manufacturing process and indirectly for the system and equipments cleaning.
DATE: July 27, 2017TIME: 9:00AM PT, 11:00AM CT, 12:00PM ETDo you have inconsistent results freeze drying samples? Are some of your samples too challenging? Is your freeze dry cycle taki...
DATE: July 19, 2017TIME: 7:00am PT, 10:00am ET, 4:00pm CETAccording to a recent report, 79% of FDA 483 Warning Letters issued in 2016 cited data integrity. In their guidance on dat...
DATE: September 20th, 2016TIME: 7:00AM PST, 10:00AM ETThere is a growing trend towards developing in vitro cell models that recapitulate the in vivo environment in basic research,...
DATE: September 8, 2016
TIME: 8:00am PST, 11:00am EST
The FDA’s 21 CFR Part 11 guidance on the use of electronic records for data retention or submission is clear. With ...
April 14, 2016, 7:00am PT, 10:00am ET, 2:00pm GMT
Whether cells are being used to manufacture a therapeutic drug product or for pharmacology, measuring the cell viability and concentration...
DATE: December 9, 2015
TIME: 8am Pacific, 11am Eastern
Pharmaceutical product quality, effectiveness and shelf life depends significantly on the water content in these products, which mak...
October 7, 2015, 8:00am PT, 11:00am ET, 3:00pm GMT
There are many laboratory Total Organic Carbon (TOC) analyzers available, most of which appear to be suitable for pharmaceutical QC use, ...
Is your lab constantly challenged by case back log while trying to validate new methods to identify designer drugs? Your challenge is common to many forensic toxicology labs around the world....
Pre-recorded webinar available for immediate playback.
Traditional method development, in which an LC method is developed principally by trial-and-error, is time consuming and may not resu...
DATE: July 27, 2017TIME: 9:00AM PT, 11:00AM CT, 12:00PM ETDo you have inconsistent results freeze drying samples? Are some of your samples too challenging? Is your freeze dry cycle taki...
DATE: July 19, 2017TIME: 7:00am PT, 10:00am ET, 4:00pm CETAccording to a recent report, 79% of FDA 483 Warning Letters issued in 2016 cited data integrity. In their guidance on dat...
DATE: September 20th, 2016TIME: 7:00AM PST, 10:00AM ETThere is a growing trend towards developing in vitro cell models that recapitulate the in vivo environment in basic research,...
DATE: September 8, 2016
TIME: 8:00am PST, 11:00am EST
The FDA’s 21 CFR Part 11 guidance on the use of electronic records for data retention or submission is clear. With ...
April 14, 2016, 7:00am PT, 10:00am ET, 2:00pm GMT
Whether cells are being used to manufacture a therapeutic drug product or for pharmacology, measuring the cell viability and concentration...
DATE: December 9, 2015
TIME: 8am Pacific, 11am Eastern
Pharmaceutical product quality, effectiveness and shelf life depends significantly on the water content in these products, which mak...
October 7, 2015, 8:00am PT, 11:00am ET, 3:00pm GMT
There are many laboratory Total Organic Carbon (TOC) analyzers available, most of which appear to be suitable for pharmaceutical QC use, ...
Is your lab constantly challenged by case back log while trying to validate new methods to identify designer drugs? Your challenge is common to many forensic toxicology labs around the world....
Pre-recorded webinar available for immediate playback.
Traditional method development, in which an LC method is developed principally by trial-and-error, is time consuming and may not resu...