Facilities & Quality Systems
State-of-the-art GMP manufacturing with world-class quality assurance
State-of-the-art GMP manufacturing with world-class quality assurance
GMP-compliant facilities designed for pharmaceutical excellence
100+ Tons
Monthly production capacity across multiple product lines
50+
Specialized R&D projects completed successfully
GMP
Good Manufacturing Practice compliance maintained
Worldwide
Serving pharmaceutical companies globally
Advanced infrastructure supporting pharmaceutical manufacturing
Dedicated manufacturing units for Active Pharmaceutical Ingredients with advanced processing equipment and controlled environments.
Specialized units for manufacturing high-purity intermediates with precision control and quality monitoring.
State-of-the-art analytical laboratories equipped with advanced instrumentation for comprehensive quality testing.
Controlled storage facilities with proper environmental monitoring and inventory management systems.
Comprehensive quality assurance ensuring product excellence
All manufacturing processes strictly follow Good Manufacturing Practice guidelines with comprehensive documentation and standard operating procedures.
Complete technical documentation including Drug Master Files (DMF), Certificates of Analysis (CoA), and Material Safety Data Sheets (MSDS).
Rigorous quality control testing at every stage of manufacturing with batch-to-batch consistency and reproducibility.
Experienced quality assurance professionals with deep expertise in pharmaceutical regulations and quality standards.
Advanced technologies and expertise driving innovation
Expertise in complex organic synthesis, process optimization, and scale-up from laboratory to commercial scale.
Advanced process development capabilities with focus on efficiency, yield optimization, and cost-effectiveness.
Comprehensive analytical testing including method development, validation, and stability studies.
Flexible contract manufacturing services tailored to specific customer requirements and timelines.
Comprehensive regulatory support including dossier preparation and compliance documentation.
Efficient supply chain management with global logistics capabilities and timely delivery.
State-of-the-art equipment ensuring precision and efficiency
Meeting international standards and regulatory requirements
Good Manufacturing Practice compliance with regular audits and continuous improvement programs.
ISO 9001:2015 Quality Management System certification ensuring consistent quality standards.
Compliance with international pharmaceutical regulations including US FDA, EMA, and other global standards.
Environmental management systems ensuring sustainable manufacturing practices and waste management.
Partner with Acta PharmaChem for reliable, high-quality pharmaceutical manufacturing backed by world-class facilities and expertise.