Be Audit-Ready with Our Comprehensive 40+ Point Checklist that covers key areas auditors typically focus on during a pharmaceutical industry audit.
Use it to identify gaps, implement corrective measures, and fortify your CAPA process to ensure compliance and continuous improvement in pharmaceutical operations.
Ensure all records are complete, accurate, and easily accessible.
Evaluate the efficiency and effectiveness of your processes and systems.
Verify adherence to all relevant regulations and standards.
Assess the condition of your facilities and the competence of your staff.
Check the effectiveness of internal and external communication channels.
Ensure ongoing tracking and resolution of CAPAs to maintain compliance.
Download other Audit Readiness checklist catering to different requirement
Build understanding on the recent FDA observations in cleaning validation.
Build understanding on the recent FDA observations in cleaning validation.
Build understanding on the recent FDA observations in cleaning validation.
Build understanding on the recent FDA observations in cleaning validation.
Build understanding on the recent FDA observations in cleaning validation.
Read about these 7 mistakes which should be at the top of your mind when selecting equipment sampling locations.
Learn how to set limits for Multi-API Products.
Introduction to Cleaning Validation
Your guide to everything API calculation related.
Understand the ins and outs of residue limits relating to Common Blend
Get a breakdown of all things residue limit related.
Find out about the latest regulations and trends in cleaning validation
Learn how to set residue limits for cleaning agents.
Find out about the most important measures to adhere to when limit-setting.
300+ pharma facilities globally use Leucine to stay compliant. Speak with one of the expert consultants at Leucine to know how.