SQA Quality College

In Person: 12-13 and 16-17 March 2023 in National Harbor, MD, USA
Virtual: 20-21 and 28-30 March 2023

March Quality College featured in-person courses and virtual courses. In-person courses were held in conjunction with the 7th Global QA Conference and 39th SQA Annual Meeting.

Visit the Quality College home page  for information on upcoming courses.

Registrants of the September 2022 Quality College may access course materials and certificates of attendance in the Online Learning Center.

Need a look back?  Quality College History

Please note that individual courses offered 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

 

Sunday, 12 March 2023

Two-day Courses, First Day | 8:00 AM - 5:00 PM EDT
GLP 101 — Basic Training in Good Laboratory Practice
GCP 101 — Understanding the Basics

One-day Courses | 8:00 AM - 5:00 PM EDT
GCP 301 — Advanced Training
CAPA 101 — Problem Definition – Beyond Human Error
GEN 111 — Critical Thinking for Quality and Compliance - CANCELLED

Half-day Courses | 1:00 - 5:00 PM EDT
PV 101 — NEW — Pharmacovigilance Auditing - Basic Training
GMP 202 — NEW — Chemistry, Manufacturing, and Controls Strategies to Assure Quality While Accelerating Drug Development

Sunday Breaks (EDT)
7:00-8:00 AM —Light Breakfast
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break
 

Monday, 13 March 2023

Two-day Courses, Second Day | 8:00 AM - 5:00 PM EDT
GLP 101 — Basic Training — Continued from Monday
GCP 101 — Understanding the Basics — Continued from Monday

One-day Courses | 8:00 AM - 5:00 PM EDT
GEN 211 — NEW — Quality Management - Ethics Meets Compliance
CAPA 201 — CAPA Creation and Effectiveness - Beyond Training
GMP 101 — GMP Foundations

Half-day Courses | 8:00 AM - 12:00 PM EDT
GLP 102 — Lies, Deceit, and Drift: The Creation of the FDA GLPs and Why They Are Still Relevant Today
GEN 209 — Guerilla Tactics for Quality Leadership

Half-day Courses | 1:00 - 5:00 PM EDT
GLP 103 — Basic GLP Archiving - What you need to know about GLP-compliant archives
CSV 205 — Over the River and Through Woods: Following the Audit Trail

Monday Breaks (EDT)
7:00-8:00 AM —Light Breakfast
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break
 

Thursday, 16 March 2023

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

Half-day Courses | 1:30 - 5:30 PM EDT
GLP 106 — NEW — FDA GLP Preamble Overview 
GEN 101 — QA Consulting
GCP 207 — NEW — You Suspect Fraud or Misconduct in Your Clinical Trial: Now What?
GCP 208 — NEW — Maximizing Risk Management in Your GCP SOPs

Thursday Breaks (EDT)
12:30-1:30 PM — Lunch
3:30-3:45 PM — Break
 

Friday, 17 March 2023

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

One-day Courses | 8:00 AM - 5:00 PM EDT
GLP 105 — Introduction to FDA GLP Bioresearch Monitoring Compliance Program
GCP 201 — Hot Topics & Industry Trends

Half-day Course | 8:00 AM - 12:00 PM EDT
GEN 104 — The Three Cs of SOPs: Clear, Concise, and Compliant in a Regulatory Setting - CANCELLED

Friday Breaks (EDT)
7:00-8:00 AM —Light Breakfast
10:00-10:15 AM — Break
12:00-1:00 PM — Lunch
3:00-3:15 PM — Break

 

Virtual Courses

 

Monday-Tuesday, 20-21 March 2023

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

Break: 12:00-12:30 PM EDT
 

Tuesday-Thursday, 28-30 March 2023

Three Partial Days | 10:00 AM - 4:00 PM EDT  |  Two-day Registration Rates
CSV 101 — Basic Concepts in Computer Validation

Break: 12:00-12:30 PM EDT
 

Questions should be sent to Courtney Thompson ([email protected]) or Lynne Valentic ([email protected]).

Gaylord National Resort Waterfront
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.