Webinars

Archived ECC Webinars

ECC # DATE TITLE Instructor(s)
ECC-643 2024-10-15 A Roadmap to a Successful Contamination Control Strategy (CCS): Covering Annex I Updates and FDA Warning Letters and 483’s Jim Polarine
ECC-639 2024-10-09 FDA Contract Manufacturing Arrangements for Drugs: Quality Agreements - Their Relationship to Microbiological Issues Barry A. Friedman Ph.D
ECC-644 2024-10-08 HVAC and GMP Environmental Control – for Pharmaceutical Clean Rooms Roger Cowan
ECC-641 2024-10-03 Investigating OOS results Danielle DeLucy
ECC-638 2024-10-02 Annual Laboratory Microbiology Training Barry A. Friedman Ph.D
ECC-637 2024-10-01 Bioburden Control of Non-Sterile Drug Substances and Products– A New USP General Information Chapter Barry A. Friedman Ph.D
ECC-636 2024-09-26 Process Simulation Testing for Aseptically Filled Products Barry A. Friedman Ph.D
ECC-629 2024-09-25 How to Remediate Microbial Contamination of Process Equipment Paul Lopolito,Brian Bosso
ECC-635 2024-09-24 VALIDATION MASTER PLANNING (DEVELOPING A COMPREHENSIVE VALIDATION PACKAGE) Barry A. Friedman Ph.D
ECC-634 2024-09-17 A Risk Assessment Approach to Address Fungal Spore Contamination in a Cell and Gene Therapy Cleanroom Jim Polarine
ECC-633 2024-09-05 TERMINALLY STERILIZED PHARMACEUTICAL PRODUCTS—PARAMETRIC RELEASE (NEW USP<1222>, November 2019) AND ITS RELATIONSHIP TO THE NEW BRITISH TERMINAL STERILIZATION METHODOLOGY (March 2019) Barry A. Friedman Ph.D
ECC-632 2024-09-04 Pharmaceutical Compressed Air – Quality GMP Standards and Requirements Roger Cowan
ECC-628 2024-08-28 Derouging and Passivation of Stainless-Steel Equipment Paul Lopolito,Dijana Hadziselimovic
ECC-627 2024-08-27 Risk Management of Raw Materials in a GMP Environment Barry A. Friedman Ph.D
ECC-625 2024-08-22 Effective Batch Record Review Danielle DeLucy
ECC-624 2024-08-21 THE BACTERIAL ENDOTOXINS TEST (ISSUES AND SOLUTIONS) TO INCLUDE THE ISSUE OF LOW ENDOTOXIN RECOVERY (LER) AND TR 82 (PDA) AND GENERAL INFORMATION CHAPTER <1085> Barry A. Friedman Ph.D
ECC-626 2024-08-15 Development of a Steam Autoclave Sterilization Validation Plan Barry A. Friedman Ph.D
ECC-622 2024-08-13 Hot Topics in the Cleanroom Industry, Biodecontamination of RABS and Isolators, Materials Transfer and Disinfectant Field Trials Jim Polarine
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