Join us for our workshop on bioanalytical methods for qualitative and quantitative analysis of proteins. This half-day workshop has been put together in collaboration with Shimadzu Scientific Instruments and we hope to share with you new insights on emerging methods of bioanalysis
The ACT Annual Meeting offers an opportunity for toxicologists preparing for the challenges and decisions that will affect public health and safety in years to come. The meeting will include a wide range of scientific programs, welcome reception and dinner, the popular poster session reception, awards ceremony, and luncheon, distinguished speakers, and networking events.
The AAPS PharmSci 360 Annual Meeting, held in Washington D.C. on November 4th-7th, this year offers robust tracks covering all aspects of the pharmaceutical sciences, hundreds of exhibitors with dozens of additional learning opportunities, thousands of scientific posters featuring the latest, most innovative research in the field, and unlimited networking opportunities to build on existing relationships and grow new ones.
WuXi AppTec Laboratory Testing Division’s analytical science leaders will share insights on overcoming common issues faced during impurity research, discuss ways to improve efficiency, and share the latest new technologies for accelerating development while at the AAPS PharmSci 360 Annual Meeting.
Dr. Caster will help to establish WuXi AppTec’s one-stop service for US submissions, and she will act as a subject matter expert for US regulatory affairs.
Dr. Guangcheng Zheng will extend our Analytical Services and manage ongoing collaboration for clients.
WuXi AppTec Laboratory Testing Division returns for the Safety Pharmacology Society (SPS) Annual Meeting, September 30 – October 3, 2018.
The SPS Annual Meeting, held in Washington, DC, this year, embraces a dynamic forum for best practice sharing within industry, CRO’s, academics and regulators, a vast array of continuing education courses, breakout sessions, poster presentations, and an expo. The meeting brings together scientists from the regulatory and CRO industry and academia.
The team of scientists at WuXi AppTec Laboratory Testing Division conduct a full scope of in vitro and in vivosafety pharmacology studies to assess the potential for toxicity across major therapeutic areas, including cardiovascular, gastrointestinal, renal, and the central nervous system.
Stop by the WuXi AppTec booth #313 to meet their experts and discuss your drug development needs. The team will supply guidance, and all the services you will need for your IND/NDA submission. While at booth #313, you can also obtain a copy of poster #0150, Titled: Comparison of Different QTc Formula for Correction of QT interval in Cynomolgus Monkeys.
To schedule a meeting with WuXi AppTec, please contact Lindsey Schwenk.
We are pleased to announce that John Pirro has joined our team as a Senior Director in WuXi AppTec Laboratory Testing Division’s Large Molecule Bioanalytical Services.
We are pleased to announce that Dr. Mark Walker has joined our team as Senior Technical Director in the WuXi AppTec Laboratory Testing Division’s Toxicology Services Department.
This is an unprecedented time for innovation in life sciences — from advancements in precision medicine to artificial intelligence to advanced diagnostics, and so much more. In order to keep up with the quick pace of this evolution, WuXi AppTec’s Laboratory Testing Division (LTD) has expanded its footprint to create even more opportunities for its global partners to address unmet medical needs through the development of novel medicines.
LTD recently doubled the size of its US facility in Cranbury, New Jersey to over 115,000 square feet, expanding its open-access technology platform and integrated services and positioning the company to collaborate and innovate with partners to create disruptive technologies. Combined, LTD’s Plainsboro and new Cranbury operations will represent one of the largest laboratories in the US for preclinical and clinical drug development testing. The expansion of the capabilities in New Jersey is the latest example of LTD’s commitment to accelerate drug development around the world, and will allow its team to deliver high quality service with faster turnaround times, better leverage the resources and expertise of the local pharmaceutical and biotechnology community, and develop a stronger connection with customers.