Microbiology News : veterinary, Apr 2019
Corning® Gosselin™ PET Storage Bottles, Break Resistant and as Transparent as Glass
23 Apr 2019 | F&BCPVCC
Corning® Gosselin™ octagonal PET storage bottles are available in 125ml to 1litre and either sterile or non sterile. more...
2018 A Year of Microbiome Investments - Infographic
08 Apr 2019 | F&BCPV
Microbiome Invest 2019 promotes partnerships and showcases the latest innovation in the microbiome field, this infographic highlights the key money movements for this sector in 2018. more...
MiDOG® Launches NGS Test for ID and AMR for Dogs
03 Apr 2019 | V
MiDOG® has worked with many vets to procure clinical data and built its proprietary, reference databases on healthy dogs. The comprehensive report provided to the vet not only shows the absolute abundance of bacteria and fungi, but it shows the data in comparison to healthy canines. more...
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LATEST MICROBIOLOGY NEWS
- AOAC Approves Modifications to iQ-Check E. coli O157:H7 and iQ-Check STEC VirX and SerO Kits
- VeraTest Biotin and VeraPrep Biotin Address Biotin Interference in Diagnostic Tests
- CE-Marked Immunoassays for Borrelia and EBV on EUROIMMUN RA Analyzer 10
- IDEXX Legiolert® Receives AFNOR ‘NF Validation’ Certification
- Virus Concentration - Faster, Easier, Better
- Increasing Throughput with INTEGRA’s VIAFLO 96 Channel Pipette
- New Microbroth Dilution Plates Provide Gold Standard-level MIC Accuracy for MDROs
- SampleReady® Pre-Weigh Soluble Media Pouches
- A New Technology Sheds Light on Salmonella and Listeria
- Bio-Rad To Launch New Droplet Digital PCR Kit to Detect STEC in Food
MICROBIOLOGY EVENTS
- Cleanroom Microbiology – A Foundational Introduction
- Microbiological cGMP Requirements for the Non-Sterile and Aseptic Fill ‘n Finish Environment
- IAFP Annual Meeting 2019
- Manufacturing Sterile Products Training
- Investigating FDA Data Integrity Regulatory Issues in a Manufacturing/Laboratory Environment
- 2019 USP <60> Microbiological Examination of Nonsterile Products Tests for B Cepacia Complex
- GMP Data Integrity Best Practices and Regulatory Expectations for the Pharmaceutical Industry
- Measuring CAPA Effectiveness: Critical Tips in Getting the Right CAPA and Showing It Works
- Implementing a Robust Cleaning and Disinfection Program & The Use of USP 1072, 1227 & 51
- Microbiological Out of Spec and Out of Trend Results in Sterile and Non-Sterile Production