GMP Standards & Regulatory Commitment
Our quality management system covers the complete product lifecycle — from supplier qualification and raw material testing through manufacturing, QC release and post-market surveillance.
GMP Manufacturing
Production areas designed to Local GMP guidelines. Every batch produced to a pre-approved Batch Manufacturing Record with full in-process documentation.
In-House QC Laboratory
Qualified pharmacists perform testing on all incoming raw materials, in-process samples and finished products against BP/USP specifications before any batch is released.
DRAP Registration
All 30+ products registered with DRAP. DML No. 000742 maintained under the Drugs Act 1976. All required inspections and renewals completed with no adverse findings.
Batch Traceability
Complete Batch Manufacturing Records for every production batch. Full traceability from raw material receipt through to finished product dispatch to distributors.
SOPs & Document Control
Comprehensive SOP library covering manufacturing, QC, cleaning and safety operations. Controlled document management with version control and training records.
CAPA & Improvement
Formal deviation reporting, root cause analysis and Corrective & Preventive Action programme. Annual product quality reviews and trend monitoring.
Storage & Cold Chain
Temperature and humidity-monitored storage areas validated per product requirements. Products dispatched only to DRAP-licensed distributors.
Supplier Qualification
Raw materials sourced from approved, qualified suppliers. Incoming materials tested against specification and Certificate of Analysis verified before use.
Recall System
Documented product recall procedure. Complete distribution records maintained for all batches enabling targeted and effective recall if ever required.
ISO Certifications & Accreditations
All four international management system certifications issued by Ethical Certifications Pvt. Limited, accredited by PNAC (Pakistan National Accreditation Council) on ISO/IEC 17021-1:2015. All certificates valid until 06 July 2026.
Certified for manufacturing of pharmaceutical products. Demonstrates that Paradise Pharma's quality management processes meet international standards for consistent product quality and customer satisfaction.
Certified for environmental management in pharmaceutical manufacturing. Demonstrates our commitment to minimising environmental impact and responsible waste management.
Certified for occupational health and safety management. Demonstrates our commitment to worker safety, hazard identification and risk reduction in our manufacturing environment.
Certified under the Hazard Analysis and Critical Control Points system. Ensures product safety through systematic hazard identification and control at critical process points.