ECCWebinars

We provide the pharmaceutical, biotech and medical device industries with leading edge webinars led by experts in their fields.

[ECCWebinars @ECCWebinars]

Cleaning and Cleaning Validation https://t.co/X2SdMSRKIW

[ECCWebinars @ECCWebinars]

Best Practices for Cleaning Validation Swab Sampling and Recovery Studies https://t.co/drQfyBar1o

[ECCWebinars @ECCWebinars]

Debates and Challenges Concerning Disinfectant Validation and Methods to Circumvent Them https://t.co/H8LMHFcKs1

[ECCWebinars @ECCWebinars]

EMA’s New 2019 Guideline on Sterilization of the Medicinal Product, API, Excipient and Primary Container – A Comparison and Contrast to FDA, USP, PDA and Health Canada Methods, Effective October 2019 https://t.co/DFlZYh9bTk

[ECCWebinars @ECCWebinars]

Development of a Steam Autoclave Sterilization Validation Plan https://t.co/YT8fmbgilg

[ECCWebinars @ECCWebinars]

Antimicrobial Effectiveness (USP)and Its Testing https://t.co/FRvjPWidi9

[ECCWebinars @ECCWebinars]

Pharmaceutical Compressed Air – Quality GMP Standards and Requirements https://t.co/OKfrTzYPeF

[ECCWebinars @ECCWebinars]

Good Laboratory Practices (GLP) vs. Good Manufacturing Practices (GMPs)– A Comparison and Contrast– “Why One Should Use Only GMP Facilities for Manufacturing and Testing” https://t.co/qodHshvxeR

[ECCWebinars @ECCWebinars]

Monitoring of Bioburden – How to Manage and Control Contamination within Non-Sterile and Sterile Products https://t.co/HK9SKj4552

[ECCWebinars @ECCWebinars]

DEVELOPING THE KEY ELEMENTS OF A PROCESS VALIDATION PLAN https://t.co/c6gqlUgzsB

[ECCWebinars @ECCWebinars]

Microbial Data Deviation Investigations — Latest FDA & ICH Requirements and Guidance https://t.co/LmV5bOmaHy

[ECCWebinars @ECCWebinars]

The Waiting Is Over – A New General Chapter,USP,Burkholderia cepaciaIs On The Horizon (December 2019 to issue) https://t.co/aaejzoTmKK

[ECCWebinars @ECCWebinars]

GMP Environmental Monitoringfor Pharmaceutical Clean Rooms https://t.co/SOHfVIQetn

[ECCWebinars @ECCWebinars]

Understanding and Troubleshooting Pharmaceutical Water Systems https://t.co/ME0Vsa7Byv

[ECCWebinars @ECCWebinars]

Risk Management of Data IntegrityTo Include FDA, WHO and EMA’s Latest Guidances for Industry https://t.co/Yncze87aF1

[ECCWebinars @ECCWebinars]

GMPs for MICROBIOLOGISTS — The Manufacturing Environment https://t.co/hCnKEGbC4M

[ECCWebinars @ECCWebinars]

Contamination Control Strategies: Facts and Sciences to Consider https://t.co/4I1ZGrCBaB

[ECCWebinars @ECCWebinars]

Regulatory Aspects of Microbiology in a Non-Sterile Environment https://t.co/5cijXscpqA

[ECCWebinars @ECCWebinars]

THE BACTERIAL ENDOTOXINS TEST (ISSUES AND SOLUTIONS) — TO INCLUDE THE ISSUE OF LOW ENDOTOXIN RECOVERY (LER) AND TR 82 (PDA) https://t.co/E22YnHwffK

[ECCWebinars @ECCWebinars]

CMO Supplier Quality Agreements – How to Comply with new FDA and EU Guidelines for Contract Drug Manufacture https://t.co/cSPMisUZSP