pathwise.com Open in urlscan Pro
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Submitted URL: https://fti8clgbb.cc.rs6.net/tn.jsp?f=001USG4aSnfIN67wjErWE4HlKB1E_n67F8T705K2NWJ3SuxbGoFw1MPpW5t8q7SDqRwxE4twyPgvFOJUHZwGSP5...
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Text Content

 * ePath Online Training
   * ePath Corporate Subscriptions
   * All eLearning Modules
   * Web Based Training for Compliance
     * Current Good Manufacturing Practices- cGMP
     * Quality System Regulation- QSR
     * Good Clinical Practices- GCP
     * Good Documentation Practices- GDP
     * Data Integrity
     * Biologics
     * Combination Products
     * Electronic Records and Signatures
     * ISO 13485
     * ISO 17025
     * EU MDR 2017/745
   * Web Based Training for Quality Systems
     * Intro to Investigations & CAPA
     * Corrective Action or Correction- Which is it?
     * Why Do We Triage?
     * Effectiveness Checks
     * Trending in Root Cause Analysis
     * Intro to Technical Writing Principles
     * Intro to Quality Risk Management
     * Intro to Quality Change Control
     * Intro to Design Control
     * Intro to Human Factors and Performance
     * Inspection Readiness
   * Web Based Training for Regulations
   * Web Based Training for Productivity
     * Effective Meeting Management
     * Microproject Management Web Based Training
   * Webinars
     * Featured Webinar
     * Webinar Memberships
     * On Demand Webinars
 * Accreditation
   * Digital Badges from PathWise
 * Instructor Led Training
   * Investigations and CAPA Training
     * CAPA Training for GCP
     * Role Based Training for Investigations and CAPA
     * Root Cause Investigation Training
     * Effectiveness Checks Training
     * Interviewing Skills Training
     * Quality Event Management Training
     * Conducting Out of Specification (OOS) Investigations Training
     * Complaint Handling Training
   * Technical Writing Principles
     * Documenting Investigations
     * Writing Standard Operating Procedures (SOPs)
     * Writing Validation Documents
     * Writing for Change Control
   * Human Factoring Records Training
   * Quality Risk Management Training
     * Risk Management for Med Device
     * Risk Management for Pharma
     * FMEA Training
     * Fault Tree Analysis (FTA) Training
   * Quality Change Control Training
     * Writing for Change Control
   * Lead Auditor Training
   * Inspection Readiness Training
   * Quality Systems and cGMP
   * Train the Trainer
   * Trainer Certification
     * Certified Trainer FAQ’s
   * Quality System Consulting
     * Remediation
     * Qualification
     * Coaching
 * Client Stories
 * About Us
   * Contact Us
   * White Papers and Help Tools
     * PathWise Partner White Papers and Help Tools
   * Public Training Events
     * Open Enrollment: March 2024
     * Open Enrollment: August 2024
     * Open Enrollment: December 2024
   * PathWise Management Team
   * PathWise Staff
   * PathWise Team of Trainers
   * Careers
   * PathWise Industry News

Select Page
 * ePath Online Training
   * ePath Corporate Subscriptions
   * All eLearning Modules
   * Web Based Training for Compliance
     * Current Good Manufacturing Practices- cGMP
     * Quality System Regulation- QSR
     * Good Clinical Practices- GCP
     * Good Documentation Practices- GDP
     * Data Integrity
     * Biologics
     * Combination Products
     * Electronic Records and Signatures
     * ISO 13485
     * ISO 17025
     * EU MDR 2017/745
   * Web Based Training for Quality Systems
     * Intro to Investigations & CAPA
     * Corrective Action or Correction- Which is it?
     * Why Do We Triage?
     * Effectiveness Checks
     * Trending in Root Cause Analysis
     * Intro to Technical Writing Principles
     * Intro to Quality Risk Management
     * Intro to Quality Change Control
     * Intro to Design Control
     * Intro to Human Factors and Performance
     * Inspection Readiness
   * Web Based Training for Regulations
   * Web Based Training for Productivity
     * Effective Meeting Management
     * Microproject Management Web Based Training
   * Webinars
     * Featured Webinar
     * Webinar Memberships
     * On Demand Webinars
 * Accreditation
   * Digital Badges from PathWise
 * Instructor Led Training
   * Investigations and CAPA Training
     * CAPA Training for GCP
     * Role Based Training for Investigations and CAPA
     * Root Cause Investigation Training
     * Effectiveness Checks Training
     * Interviewing Skills Training
     * Quality Event Management Training
     * Conducting Out of Specification (OOS) Investigations Training
     * Complaint Handling Training
   * Technical Writing Principles
     * Documenting Investigations
     * Writing Standard Operating Procedures (SOPs)
     * Writing Validation Documents
     * Writing for Change Control
   * Human Factoring Records Training
   * Quality Risk Management Training
     * Risk Management for Med Device
     * Risk Management for Pharma
     * FMEA Training
     * Fault Tree Analysis (FTA) Training
   * Quality Change Control Training
     * Writing for Change Control
   * Lead Auditor Training
   * Inspection Readiness Training
   * Quality Systems and cGMP
   * Train the Trainer
   * Trainer Certification
     * Certified Trainer FAQ’s
   * Quality System Consulting
     * Remediation
     * Qualification
     * Coaching
 * Client Stories
 * About Us
   * Contact Us
   * White Papers and Help Tools
     * PathWise Partner White Papers and Help Tools
   * Public Training Events
     * Open Enrollment: March 2024
     * Open Enrollment: August 2024
     * Open Enrollment: December 2024
   * PathWise Management Team
   * PathWise Staff
   * PathWise Team of Trainers
   * Careers
   * PathWise Industry News


WHAT’S THE RIGHT NUMBER OF CAPAS?

Spoiler alert- it’s not an exact number, and that number isn’t zero. The right
number of CAPAs will vary organization to organization based on several factors,
which we will outline for you below to take into consideration when developing
CAPA targets for your business.

Read about these steps, to right size your CAPA workload:

 1. Calibrate What a CAPA Is and Isn’t
 2. Evaluate the Sources of Your Current CAPAs
 3. Evaluate the Time Spent in Firefighting Mode
 4. Evaluate How Much Time is Actually Spent on CAPAs
 5. Calculate Approximate CAPA Capacity
 6. Apply The Information

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