Available Courses

Results (25)




Course Title Course Date Location
Intro to Medical Device Submission - 510(k)s, PMAs & Exemptions May 04, 2020 - May 05, 2020 Los Angeles, CA United States of America
Introduction to Medical Combination Products May 06, 2020 - May 08, 2020 Los Angeles, CA United States of America
Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products May 18, 2020 - May 19, 2020 Los Angeles, CA United States of America
Computer System Validation Jul 13, 2020 - Jul 14, 2020 Los Angeles, CA United States of America
Writing Effective SOP and Other Process Documents Jul 20, 2020 - Jul 21, 2020 Los Angeles, CA United States of America
Technical Writing for Pharma, Biotech and Med Devices Jul 22, 2020 - Jul 24, 2020 Los Angeles, CA United States of America
Integration of Risk Management Principles and Activities into the Quality System Jul 27, 2020 - Jul 28, 2020 Los Angeles, CA United States of America
Medical Device Process Validation Training for Professionals Jul 29, 2020 - Jul 31, 2020 Los Angeles, CA United States of America
US Cosmetic Regulation: FDA CFR Title 21 Training Aug 19, 2020 - Aug 21, 2020 Los Angeles, CA United States of America
Good Manufacturing Practices Training | GMP Course Aug 24, 2020 - Aug 26, 2020 Los Angeles, CA United States of America
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Sep 14, 2020 - Sep 15, 2020 Los Angeles, CA United States of America
Lyophilization Technology-Application of Scientific Principles Sep 17, 2020 - Sep 18, 2020 Los Angeles, CA United States of America
GMPs for OTC & Cosmetic Products - US and Global Requirements Sep 21, 2020 - Sep 22, 2020 Los Angeles, CA United States of America
Overview of FDA Regulatory Compliance for Medical Devices Sep 24, 2020 - Sep 25, 2020 Los Angeles, CA United States of America
Auditing and Qualifying Suppliers and Vendors Oct 15, 2020 - Oct 16, 2020 Los Angeles, CA United States of America
Best Practices for an Effective Cleaning Validation Program Oct 15, 2020 - Oct 16, 2020 Los Angeles, CA United States of America
Pharmaceutical Production Batch Record Review | Training Oct 19, 2020 - Oct 20, 2020 Los Angeles, CA United States of America
Quality Assurance/Quality Control for Biologics and Biopharmaceuticals Oct 19, 2020 - Oct 21, 2020 Los Angeles, CA United States of America
Process Validation for Drugs and Biologics Oct 19, 2020 - Oct 20, 2020 Los Angeles, CA United States of America
Basic GMP Training for the QC Laboratory Oct 21, 2020 - Oct 22, 2020 Los Angeles, CA United States of America
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Oct 21, 2020 - Oct 23, 2020 Los Angeles, CA United States of America
Qualifying, Management and Auditing of Contract Manufacturing Organizations Oct 22, 2020 - Oct 23, 2020 Los Angeles, CA United States of America
FDA Inspections - What Regulators Expect and How to Prepare Nov 09, 2020 - Nov 10, 2020 Los Angeles, CA United States of America
Development and Validation of Bioanalytical Assays for Biologics Quantitation and Immunogenicity Assays Dec 03, 2020 - Dec 04, 2020 Los Angeles, CA United States of America
Preparing the CMC Section for NDAs/INDs/CTDs Dec 07, 2020 - Dec 08, 2020 Los Angeles, CA United States of America