Internationally Recognized Standards
Lab Certified

Pharmaceuticals & Healthcare Compliance

Scientific screening of gelatin capsules, excipients, active ingredients (APIs), and medicine manufacturing plants.

Regulatory Standard: OIC/SMIIC 50 & MS 2424
Validity: Global Customs Recognition
Pharmaceuticals & Healthcare Compliance

Program Overview & Conformity Mandate

Pharmaceutical products require specialized dual-competence audits: strict biomedical safety and total shariah conformity. Our inspection protocols analyze APIs (Active Pharmaceutical Ingredients), binders, coatings, and oral dosage forms.

Gelatin Traceability in Capsule Shells

Capsule shells represent the primary vulnerability in healthcare. We enforce batch-wise molecular sequencing to verify bovine-only origins sourced exclusively from audited certified slaughter facilities.

Vaccines, Syrups & Biologics

Biomedical fermentation media, stabilizers, and oral suspension liquid formulations are verified to guarantee zero synthetic alcohol stabilization or forbidden enzymes.

Standard Audit & Verification Protocol

01
Step 1: Pharmacopoeia & Excipient Formulation Review
02
Step 2: Physical Inspection of Cleanrooms & Air Handling Units
03
Step 3: Quantitative PCR Gelatin DNA Testing
04
Step 4: Compliance Directorate Authorization

Preliminary Documentation Required

Prepare the following manufacturer files for fast-track stage 1 audit submission:

Finished Formulation Batch Manufacturing Records (BMR)
Gelatin Source Origin & Slaughter Certificates
Drug Master File Excipient Safety Declarations
Valid GMP (Good Manufacturing Practice) License

Apply for Pharmaceuticals & Healthcare Compliance

Our technical audit desk will respond with scope analysis within 48 business hours.