LC a LCMS webináře - 47. týden

V týdnu od 16. listopadu 2020 Vás čekají v oblasti LC a LCMS následující webináře, kterých detaily a registraci najdete v sekci WEBINÁŘE:

Nově také s možností vyhledávání a filtrace v téměř 550 GC a LC webinářích.

1. Thermo Fisher Scientific: Metabolomics session 4: Chromatographic solution

2. Thermo Fisher Scientific: Proteomics session 4: Targeted proteomics

3. LCGC/Metrohm: Ion Chromatography in Pharmaceutical R&D

4. Phenomenex: HILIC - A Systematic Approach

5. Thermo Fisher Scientific: Metabolomics session 5: Compound Discoverer

6. Thermo Fisher Scientific: Proteomics session 5: Proteome Discoverer

7. LCGC/Agilent Technologies/Avantor/Merck group/Tosoh Bioscience: Biopharmaceutical Analysis Focus 2020: A Virtual Symposium - DAY 1

8. Technology Networks/Bruker: MALDI-MS-based assays for cellular drug action and transport with rapifleX MPP

9. SelectScience/Waters Corporation: Improved LC-MS analysis of oligonucleotides with next-generation chromatography

10. Agilent Technologies: Advanced Agilent QTOF Acquisition Utilities

11. SelectScience/Thermo Fisher Scientific: European LC-MS/MS Clinical Laboratory Virtual Day

12. Shimadzu Scientific Instruments: Shimadzu's LC Method Development (RP) Series - Session 1: Method Screening

13. LCGC/Agilent Technologies/Avantor/Merck group/Tosoh Bioscience: Biopharmaceutical Analysis Focus 2020: A Virtual Symposium - DAY 2

14. Separation Science/SCIEX: Extractables and Leachables in Food Contact Material

15. Separation Science/SCIEX: Screening for Extractables and Leachables: QTOF, SWATH® Acquisition and Spectral Libraries

16. LCGC/Thermo Fisher Scientific: Using Combustion Ion Chromatography to Screen for Extractable Organic Fluurine in PFAS, PFAS, FTOH, and FOSA in Water Monitoring

17. Agilent Technologies: WHEN Should I Change That: Ensuring Proper Instrument Performance

18. Agilent Technologies: Practical Approaches to Preparative Chromatography

19. LCGC/Waters Corporation: Applying ISO 10993-18 on Extractables & Leachables Characterization - Supporting the Medical Device Regulatory Pathway