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PTS was founded in 1991 an through the years it has made a name for itself by organizing vocational training courses mainly concerning the topics GMP, GCP and GLP. Last year more than 80 courses took place with a total of 2000 participants coming from pharmaceutical, active pharmaceutical ingredient more
Nearly 80 years ago, the development of the glass electrode at the former Jenaer Glaswerk SCHOTT & Gen. revolutionized chemical measuring. By using new conductive glass types it was now possible to display pH values via conventional needle galvanometers. The further company history too was marked b more
EasyDirect maintains a complete history of your entire pipette inventory including calibration certificates and verification reports more
Reliable results, easy to use, and a true bargain from the global market leader in titration: The new Eco Titrator from Metrohm is an entry-level titrator for anyone looking for maximum accuracy and reliability at an affordable price. more
eVol®, the world’s first automated analytical syringe created and manufactured by SGE Analytical Science, has been selected as a 2010 R&D100 Award winner. eVol® is a unique laboratory tool that removes the human limitation of manual liquid handling delivering significantly improved levels of accura more
Intertek announced the acquisition of Ciba Expert Services' Environmental, Safety, & Testing and Regulatory businesses, including Cantox Health Sciences and Ashuren Health Sciences. The acquisition substantially strengthens Intertek's scope and depth for regulatory consulting to meet customers' nee more
Intertek is strengthening its technical capabilities in the UK by merging two key facilities, creating a European Analytical Testing Centre of Excellence in Manchester. The resources and expertise of Intertek’s North West Technology Centre (NWTC) at Bebington and the Analytical Sciences Group (ASG) more
The Laboratory Data Integrity Guide illustrates safe ways to achieve data integrity and discusses where data integrity might be at risk. more
Businesses that utilize quality assurance systems such as GMP/GLP must check their balances regularly. The check intervals are often very short. more
Before a medicine can be approved for clinical trials, it is subjected to a tightly regulated development process monitored by the relevant bodies. more
completed her studies for a Bachelor of Science in Molecular Biotechnology from TU Dresden before graduating from the international degree programme “Molecular Medicine” at Charité – Universitätsmedizin (Berlin) with an M.Sc. in 2009. Funded by a grant from Charité, she then completed her doctoral w more
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