SQA Quality College

In Person: 6-7 and 10-11 April 2024 in Aurora, CO, USA
Virtual: 16-17 April 2024

The April 2024 Quality College featured in-person courses and one virtual course. In-person courses were held in conjunction with the 40th SQA Annual Meeting.

Please note that individual courses offer various RQAP Re-registration units, depending on the topic and length of the course. Unit categories include GCP/Non-GLP and GLP/Non-GCP.

See below for links to course descriptions.

 

 In-Person Courses

Saturday, 6 April 2024

Two-day Courses, First Day | 8:00 AM - 5:00 PM MDT
1-GLP 101: Basic Training in Good Laboratory Practice  
2-GCP 101: Understanding the Basics  
3-CAPA 102: Root Cause Analysis and the CAPA Lifecycle: Beyond Human Error and Training  

One-day Courses | 8:00 AM - 5:00 PM MDT
4-GMP 101: GMP Foundations  
5-PV 102: Pharmacovigilance Auditing - Comprehensive Basic Training  

Half-day Courses | 8:00 AM - 12:00 PM MDT
NEW! 6-GLP 205: Moving GLP Compliance from Paper to Digital  
NEW! 7-GEN 215: Building a Quality Culture  
NEW! 8-GCP 209: Challenges in Auditing Clinical Labs: Is CLIA Certification Enough?  

Half-day Courses | 1:00 PM - 5:00 PM MDT
NEW! 9-GLP 302: Quality Assurance for New Approach Methodologies  
NEW! 10-GEN 111: Critical Thinking by Design  
11-CSV 205: Over the River and Through the Woods: Following the Audit Trail  

Saturday Breaks (MDT)
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break
 

Sunday, 7 April 2024

Two-day Courses, Second Day | 8:00 AM - 5:00 PM MDT
1-GLP 101: Basic Training in Good Laboratory Practice  — Continued from Saturday
2-GCP 101: Understanding the Basics  — Continued from Saturday
3-CAPA 102: Root Cause Analysis and the CAPA Lifecycle: Beyond Human Error and Training  — Continued from Saturday

One-day Courses | 8:00 AM - 5:00 PM MDT
12-GMP 301: Advanced GMP - CANCELLED
13-GCP 201: Hot Topics & Industry Trends  
14-GEN 211: Quality Management - Ethics Meets Compliance - CANCELLED

Half-day Courses | 8:00 AM - 12:00 PM MDT
NEW! 15-PV 202: PV, QA, and AI: How to Not Do What We Have Always Done  
16-GMP 202: Chemistry, Manufacturing, and Controls Strategies to Assure Quality Whilst Accelerating Drug Development  

Half-day Courses | 1:00 PM - 5:00 PM MDT
17-GEN 102: SQA Leadership Development  
18-GLP 106: FDA GLP Preamble Overview  

Sunday Breaks (MDT)
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break
 

Wednesday, 10 April 2024

1.5 Day Course, First Day | 1:30 PM - 5:30 PM MDT
19-GMP 201: Effective GMPs  

Half-day Courses | 1:30 - 5:30 PM MDT
NEW! 20-RI 102: 5 C's to respond to an FDA-483  
21-GCP 208: Maximizing Risk Management in Your GCP SOPs  
22-GEN 101: QA Consulting  
23-GEN 209: Wily Tactics for Quality Leadership  

Wednesday Breaks (MDT)

12:30-1:30 PM — Lunch
3:30-3:45 PM — Break
 

Thursday, 11 April 2024

1.5 Day Course, Second Day | 8:00 AM - 5:00 PM MDT
19-GMP 201: Effective GMPs  — Continued from Wednesday

One-day Courses | 8:00 AM - 5:00 PM MDT
24-GLP 105: Introduction to FDA GLP Bioresearch Monitoring Compliance Program  
25-GCP 301: Advanced Training in GCP  
26-RI 106: Auditor’s Primer on the Science, Practice, and Auditing of Chromatography and Mass Spectrometry  
27-GEN 213: QMS Optimization: A Guide for Small Companies  

Half-day Course | 8:00 AM - 12:00 PM MDT
NEW! 28-GEN 216: Performing More Effective Strengths, Weaknesses, Opportunities, and Threats (SWOT) Analyses  

Half-day Course | 1:00 PM - 5:00 PM MDT
29-DEV 204: Risk Based Approach vs. Risk Management, and Determination of Acceptable Risk  

Thursday Breaks (MDT)
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break

 

 Virtual Course

Tuesday - Wednesday, 16-17 April 2024

Two Half-days | 10:00 AM - 2:30 PM EDT  |  One-day Registration Rates
30-GLP 104: Auditing Techniques  

Break: 12:00-12:30 PM EDT

 
Quality College Course

Looking for basic training in GCPs or GLPs?

SQA has its basic courses in GCP and GLP available in on-demand online formats, available to you at your convenience:

Other on-demand courses are also available on the topics of GLP Study Director and Principal Investigator Training, Introduction to 21 CFR Part 11, and Introduction to Writing Effective Compliant GLP SOPs at sqa.org/learn.