Being Prepared for an Active Shooter Incident at Workplace 2022
Read MoreUSMCA Rules, Procedures and Documentation 2022
Read MoreBacterial Endotoxin Test to Include the Latest on Low Endotoxin Recovery (LER) 2022
Read More2022 Precision Oncology Summit 2022 Salt Lake City United States
Read More33rd European Pediatrics Conference 2022
33rd European Pediatrics Conference
Read MorePharmaceutical Quality Management - Risk Management and Regulatory Compliance 2022
Read MoreMajor CGMP Issues - US FDA Concerns in 2022 2022
This webinar will evaluate the chief areas of FDA CGMP and EU compliance inspections to see actual and anticipated changes in emphasis, and how to better prepare with a company's proactive internal inspection / audit program.
Read MoreHIPAA Audit and Enforcement Update for 2022 - HHS Keeps Pressure on Access, Privacy, and Security Compliance 2022
Read MoreLead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation 2022
Read More12th International Conference on Neurological Disorders & Stroke 2022 Barcelona Spain
Read More53rd World Congress on Advanced Nursing Practices 2022 osaka Japan
The conference “53rd World Congress on Advanced Nursing Practices” will be held on May 24-25, 2022, Osaka, Japan.
Read MoreREACH and RoHS Compliance: Gain a Deeper Understanding 2022
Read MoreThe 6 Most Common Problems in FDA Software Validation and Verification 2022
This training on FDA software validation and verification will provide you the best practices necessary to ensure that all systems are validated in compliance with FDA regulations.
Read MoreRisk-Based Approach to CSV, 21 CFR Part 11 and FDA Compliance 2022
Read MoreREACH and RoHS Compliance: Gain a Deeper Understanding 2022
Read MoreAseptic Processing in the Manufacture of Biotech and Pharmaceutical Products 2022
Read MoreHow to Prepare a 510(k) Submission 2022
How to Prepare a 510(k) Submission
Product Id : MD3392
Category : FDA Compliance, Medical Devices
Presenter : Edwin Waldbusser
Scheduled On : April 21 2022 1:00 pm
US/Canada (Eastern Time - ET)
Duration : 60 Minutes
Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Program 2022
Regulatory and Testing Requirements of the Bacterial Endotoxin Testing (BET) or LAL Program
Read MoreTest Method Validation to Verify your Device Performance 2022
Product Id : MD3048
Category : FDA Compliance, Medical Devices, Quality
Presenter : José Mora
Scheduled On : April 20 2022 1:00 pm
US/Canada (Eastern Time - ET)
Duration : 60 Minutes
Analytical Instrument Qualification and System Validation 2022
Read More21 CFR Part 11 Compliance for SaaS/Cloud Applications 2022
This highly interactive two-day course uses real life examples and explores proven techniques for reducing costs, usually by two-thirds, associated with implementing, and maintaining computer systems in regulated environments.
Read MoreReduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR 2022
Read MoreSupplier and Contract Manufacturer Management for Medical Device Manufacturers 2022
Read MoreREACH and RoHS Compliance: Protecting Revenues with Advanced Compliance 2022
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