Available Courses

Results (37)




Course Title Course Date Location
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development May 17, 2017 - May 19, 2017 Los Angeles, CA United States
QA/QC Strategy for Biologics and Biopharmaceuticals May 31, 2017 - Jun 02, 2017 Los Angeles, CA United States
Auditing and Qualifying Suppliers and Vendors™ Jun 05, 2017 - Jun 06, 2017 Los Angeles, CA United States
CMC Regulatory Compliance for Biopharmaceuticals, Biosimilars and Other Biologics Jun 05, 2017 - Jun 07, 2017 Los Angeles, CA United States
Preparation of FDA Submissions and Communicating with the FDA Jun 08, 2017 - Jun 09, 2017 Los Angeles, CA United States
FDA Inspections: What Regulators Expect and How to Prepare Jun 12, 2017 - Jun 13, 2017 Los Angeles, CA United States
Pharmaceutical Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy Jun 14, 2017 - Jun 16, 2017 Los Angeles, CA United States
Stability Programs for Determining Product Shelf Life Jun 19, 2017 - Jun 20, 2017 Los Angeles, CA United States
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials Jul 17, 2017 - Jul 18, 2017 Los Angeles, CA United States
Introduction to Statistical Analysis of Laboratory Data Jul 17, 2017 - Jul 18, 2017 Los Angeles, CA United States
Biostatistics for Non-Statisticians Jul 19, 2017 - Jul 21, 2017 Los Angeles, CA United States
Good Clinical Practices & Risk Based Monitoring Jul 19, 2017 - Jul 21, 2017 Los Angeles, CA United States
Lyophilization Technology – Practical Application of the Scientific Principles Jul 20, 2017 - Jul 21, 2017 Los Angeles, CA United States
Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries™ Jul 24, 2017 - Jul 25, 2017 Los Angeles, CA United States
Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer Jul 24, 2017 - Jul 25, 2017 Los Angeles, CA United States
Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices™ Jul 26, 2017 - Jul 28, 2017 Los Angeles, CA United States
Process Validation for Drugs and Biologics Jul 26, 2017 - Jul 27, 2017 Los Angeles, CA United States
Good Laboratory Practices (GLP) for Pre-Clinical Testing Aug 07, 2017 - Aug 09, 2017 Los Angeles, CA United States
Introduction to Effective Medical Writing Aug 07, 2017 - Aug 08, 2017 Los Angeles, CA United States
The Drug Development Process - From Discovery to Commercialization™ Aug 07, 2017 - Aug 09, 2017 Los Angeles, CA United States
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries Aug 09, 2017 - Aug 11, 2017 Los Angeles, CA United States
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products Sep 07, 2017 - Sep 08, 2017 Los Angeles, CA United States
Global Review of Sunscreen Science, Products & Regulation Sep 13, 2017 - Sep 15, 2017 Los Angeles, CA United States
API & Drug Product Specifications – From Clinical Development to Market Approval Sep 18, 2017 - Sep 19, 2017 Los Angeles, CA United States
Best Practices for an Effective Cleaning Validation Program Sep 18, 2017 - Sep 19, 2017 Los Angeles, CA United States
Good Manufacturing Practices (cGMP) Oct 02, 2017 - Oct 04, 2017 Los Angeles, CA United States
The Electronic Common Technical Document (eCTD): Strategies & Tools to Build a Successful Submission Oct 23, 2017 - Oct 24, 2017 Los Angeles, CA United States
US Cosmetic Regulation - FDA CFR Title 21 Oct 25, 2017 - Oct 27, 2017 Los Angeles, CA United States
GMPs for OTC and Cosmetic Products – US and Global Requirements Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Integration of Risk Management Principles and Activities into the Quality System Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Preparing the CMC Section for NDAs/INDs/CTDs Nov 06, 2017 - Nov 07, 2017 Los Angeles, CA United States
Global Personal Care Market & Regulatory Overview Nov 08, 2017 - Nov 10, 2017 Los Angeles, CA United States
Process Validation for Medical Devices Nov 08, 2017 - Nov 10, 2017 Los Angeles, CA United States
Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications Nov 13, 2017 - Nov 14, 2017 Los Angeles, CA United States
Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Nov 15, 2017 - Nov 16, 2017 Los Angeles, CA United States
Development and Validation of Bioanalytical Assays for Biologics Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States
Validation of Computer Systems Dec 07, 2017 - Dec 08, 2017 Los Angeles, CA United States