How We Work
Quality-Driven Process
Celtic Operational Flow – WHO-cGMP & CDSCO Compliant
Our end-to-end operational framework is designed to meet global quality and regulatory benchmarks, ensuring safe, consistent, and compliant pharmaceutical solutions at every stage.
Selection of Certified & Qualified Manufacturing Partners
With a strong focus on quality and compliance, Celtic Life Science offers a diverse portfolio of pharmaceutical formulations across multiple dosage forms including tablets, capsules, syrups, injectables, nutraceuticals, and speciality medicines. Our products are developed and manufactured in accordance with international quality standards to ensure consistency, safety, and efficacy.
Cross-Functional Collaboration & Strategic Alignment
Celtic’s scientific, regulatory, quality, and operations teams work in close coordination with the manufacturing partner to finalize product specifications, regulatory pathways, development strategies, timelines, and compliance requirements.
Global API Sourcing from Approved Suppliers
Active Pharmaceutical Ingredients (APIs) are sourced exclusively from globally approved and audited suppliers, ensuring high standards of purity, potency, traceability, and compliance with international pharmacopoeial and regulatory standards.
Compilation & WHO-cGMP-Compliant Production
The product progresses through formulation finalization, pilot batch development, scale-up, and commercial manufacturing under validated, controlled, and WHO-cGMP compliant production environments.
Quality Control & Quality Assurance (WHO-cGMP / CDSCO Compliant) Celtic follows a robust Quality Management System (QMS) in line with WHO-cGMP guidelines and CDSCO requirements:
Incoming Raw Material & API Testing for identity, assay, purity, and microbiological limits In-Process Quality Control (IPQC) to monitor Critical Quality Attributes (CQAs) and Critical Process Parameters (CPPs) Finished Product Testing as per approved specifications and validated analytical methods Stability Studies conducted in accordance with ICH guidelines to establish shelf life Batch Manufacturing & Packing Record (BMR/BPR) Review prior to release Deviation, OOS/OOT Investigations and CAPA Implementation Only batches meeting all quality and regulatory criteria are approved for release.
Advanced & Patented Packaging Technology
Celtic implements innovative and patented packaging technologies designed to enhance product stability, safety, shelf life, tamper resistance, and regulatory compliance while strengthening brand integrity.
Secure & Validated Packing
Products are packed using validated, tamper-evident, and transit-secure packaging systems to ensure product integrity throughout storage, handling, and transportation.
Structured Distribution to End Users
A controlled and efficient supply chain ensures seamless distribution from Celtic Depots → Authorized Distributors → Chemists / Hospitals / Organizations → Patients, guaranteeing timely availability, safety, and trust.