Upcoming Microbiology Events : laboratory-equipment , 2019-08
Cleaning Validation; Understanding the Latest FDA, EU, EMA, Health Canada Requirements
: 13 Aug 2019
: Webinar
Sector: Clinical, Cosmetic/Personal Care, Laboratory Equipment, Other, Pharmaceutical, Veterinary, Water Type: Training
Summary : This comprehensive live training webinar is designed to provide a comprehensive review of selected regulatory documents as they relate to sampling and sampling recovery, dirty hold time, clean hold time, microbiological issues and validation maintenance. more...
Risk Management of Raw Materials in a GMP Environment
: 19 Aug 2019
: Webinar
Sector: Clinical, Cosmetic/Personal Care, Laboratory Equipment, Pharmaceutical, Veterinary, Water Type: Webinar
Summary : This live training webinar will also examine a variety of the issues surrounding raw materials to include what materials should be tested and to what extent during Phase 1, 2 and 3. 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