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NAFDAC & Compliance
Built for trust. Structured for scrutiny.
This section is designed for regulators, institutional buyers, donor organizations, and commercial partners who require clear evidence of operational integrity.
Carlos Pharmaceuticals is structured with compliance at its core—aligning processes, documentation, and quality systems with National Agency for Food and Drug Administration and Control (NAFDAC) expectations and global best practices.
Quality Systems
We operate with a quality-first mindset, embedding process discipline across production, documentation, and product lifecycle management.
From raw material intake to batch release, every stage is guided by defined controls, traceability, and accountability.
Documentation Culture
Our documentation framework is built to support transparency, audit readiness, and operational consistency.
This includes structured governance around:
- Standard Operating Procedures (SOPs)
- Batch manufacturing records
- Deviation tracking and resolution
- Controlled documentation workflows
Compliance Readiness
Carlos maintains a proactive approach to regulatory alignment, ensuring readiness for inspections, audits, and partner evaluations at all times.
Our systems are designed to demonstrate:
- NAFDAC-aligned operating standards
- Inspection preparedness
- Ongoing compliance monitoring
- Partner assurance and accountability
Compliance Framework & Documentation
NAFDAC Authority to Manufacture
NAIP Certificate
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CARLOS PIROXICAM 20mg CAPSULES
A11-101011
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CARLOS ARTEMETHER 20mg LUMENFANTRINE 120mg TABLET
A11-100914
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CARLOS TENOXICAM 20MG CAPSULE
A11-100934
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CARLOS IBUPROFEN SUSPENSION 100MG/5ML
A11-100938
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CARLOS ARTEMETHER 80mg LUMENFANTRINE 480mg TABLET
A11-100933
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CARLOS BLOOD CAPSULE
A11-101061
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PAKSIL MIST MAG TRISILICATE
A11-101062
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MYCOLUS CREAM
A11-101060
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CARLOS METHYLSALICYLATE HEAT BALM
A11-101024