Sterile manufacturing environments at medical device and pharmaceutical companies require effective cleaning and disinfection programs to maintain aseptic conditions and prevent microbial contamination. To help, laboratory testing experts will present "Clean Room Environmental Best Practices,"

Reusable Medical Device Cleaning Validation and Testing Requirements (An Industry Perspective)

Summary of Proposed Changes to 21 CFR 610: The New Scope of Cleaning Validations

New Medical Device Polymer Biocompatibility Screening Test Using Zebrafish Embryos (Danio Rerio),"

AGAWAM, Mass., Nov.