About us

“Excellence in Every Step, Quality in Every Product”

At Oceanic Pharmachem, quality is the foundation of everything we do. We are committed to delivering products that meet and exceed global standards, ensuring safety, efficacy, and regulatory compliance. Our Quality Assurance (QA) Department meticulously oversees each stage of production — from supplier qualification to final product release — to guarantee the highest level of quality for our customers.

Supplier Qualification & Audits

We work only with manufacturers who meet stringent quality criteria. Our multi-step supplier qualification process includes:

•  Self-Assessment & Documentation Review: Initial evaluation of manufacturing practices
• On-Site Audits: Comprehensive inspections to verify compliance with cGMP, ICH Q7, and other international standards
• Ongoing Supplier Monitoring: Regular audits and performance reviews to ensure continuous adherence to quality benchmarks

This rigorous approach ensures we partner with trusted manufacturers who share our commitment to excellence.

Robust Quality Management System (QMS)

We’ve implemented a comprehensive Quality Management System (QMS) that governs all aspects of product handling, documentation, and compliance. Key elements include:

• Process Validation & Control: Constant monitoring of manufacturing processes to prevent deviations
• Change Management: Careful evaluation and approval of any process changes to avoid quality compromises
• Deviation & CAPA Management: Swift identification, investigation, and resolution of quality deviations through Corrective and Preventive Actions (CAPA)

Our QMS ensures that quality is a continuous, evolving process, not just a final checkpoint.