Courses - Eventura.site

FDA Regulations and Requirements for Artificial Intelligence / Machine Learning

Analytical Instrument Qualification & Validation - Use of Excel and FDA Audit Preparation

QUALITY BY DESIGN (QBD) IN PHARMACEUTICAL AND MEDICAL DEVICE MANUFACTURING

DESIGN CONTROL 2023: PROJECT MANAGEMENT UTILIZING PRINCIPLES OF LEAN DOCUMENTS AND LEAN CONFIGURATION

ESSENTIAL EU MDR REQUIREMENTS - MINIMIZE THE RISK OF NON-COMPLIANCE

3-HOUR VIRTUAL SEMINAR ON 510(K)'S, PMA'S, IDE'S AND DENOVO'S

Establishing FDA-Compliant Product Stability Testing Program

FDA Expectations for 505(b)(2) Regulatory Pathway for New Drugs

FDA vs Health Canada - Similarities and Differences between the two Regulatory Bodies

21 CFR PART 11 COMPLIANCE FOR ELECTRONIC RECORDS AND SIGNATURES

Production and Process Controls for Medical Devices

EU's New Regulation 535/2014 On Clinical Trials - Insights Into Effective Clinical Trials

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