
Internal Halal Audit Checklist [PDF Download]
Purpose: This Internal Halal Audit Checklist is designed to help businesses conduct thorough internal audits to ensure compliance with halal standards.
Use this checklist during regular audits to ensure all aspects of your operations comply with halal standards. Check each item as ‘Compliant,’ ‘Non-Compliant,’ or ‘Not Applicable.’ Provide detailed notes and recommendations for any non-compliant items.
Download the Internal Halal Audit Checklist from AHF below!

Download Internal Halal Audit Checklist
Frequently Asked Questions (FAQs)
Q: How long does it take to obtain halal certification for pharmaceuticals?
A: The certification process typically takes 4-7 weeks, depending on document readiness, the complexity of materials, and audit scheduling.
Q: What documents are required for halal pharmaceutical certification?
A: Required documents include ingredient specifications, process flow diagrams, supplier halal certificates, and facility layout. These details help assess potential cross-contamination risks.
Q: Can a pharmaceutical product with animal-derived ingredients be certified as halal?
A: Yes, but only if the animal-derived ingredients, such as gelatin or enzymes, come from halal-certified sources. The animals must be slaughtered according to Islamic guidelines for the ingredient to be deemed halal-compliant.
Q: How are cross-contamination risks managed in halal pharmaceutical production?
A: Halal-certified manufacturers must implement strict separation protocols, including dedicated production lines or thorough cleaning of shared equipment. Regular internal audits and training on halal compliance are essential to prevent cross-contamination with non-halal substances.
Q: Are employees required to receive halal compliance training?
A: Yes, halal certification bodies require that all relevant employees undergo training on halal standards. This includes understanding the importance of avoiding cross-contamination, proper handling of halal-sensitive products, and thorough documentation procedures.