Advanced Batch Production Records Concepts

Advanced Batch Production Records Concepts

Participants will learn the importance and benefits of having and completing Batch Production Records (BPRs) and the differences/similarities/relationship to the Master Batch Records. They will also learn how and why to effectively review batch production records for accuracy and completeness for compliance with Good Documentation Practices and for Data Integrity. Participants will explore manual and digital BPRs, determine what items are included in these, and the steps that are necessary to effectively review them before reviewing an actual, internal BPR for errors, omissions, and completeness.

Audience

  • Biomanufacturing
  • Bioprocessing
  • Pharmaceutical
  • Medical Device
  • Cosmetics
  • Other FDA regulated industry sectors

Topics Include

  • Benefits of Effective BPRs
  • Regulatory Requirements for BPRs
  • Master Batch Records
  • Relationship of BPRs and MBRs
  • Content of BPRs
  • Effective Reviews of BPRs
  • Actual Review Activity of a BPR

Learning Objectives

  • Discuss the rationale for why we complete batch production records (BPRs)
  • Understand the relationship between BPRs and current Good Manufacturing Practices compliance
  • Examine regulatory aspects of BPRs
  • Review the basics of Master Production Records and BPRs
  • Explore examples of information included in BPRs
  • Compile a list of items for completing a BPR internally
  • Compile a list of objectives for reviewing a BPR internally
  • Examine an internal BPR for errors and discussion
Advanced Batch Production Records Concepts

Request this Course

Level: Intermediate

Lecture HoursLab or Activity HoursTotal

Delivery Options

Face-to-Face
Delivered in-person in a classroom or lab setting.
Hybrid
A combination of online and in-person components.
Live Instructor Led
Delivered online with a live instructor at a scheduled date and time.
Related
eLearning
Delivering a new pharmaceutical to the market is a very time-consuming and expensive process that... more
Good Laboratory Practices (GLP)
eLearning
You’re the newest member of the Quality Assurance department at CATT – the Center for the... more
Validation Fundamentals
eLearning
In this short eLearning course, you'll learn the fundamentals of process and equipment validation... more
Deliberate Documentation
eLearning
Documentation is a critical part of any manufacturing process. Every manufacturing step is... more