About Us

Quality is embedded into every aspect of our operations—from early-stage development to GMP-certified manufacturing. Our facilities, processes, and teams are structured around a deep-rooted culture of compliance and continuous improvement. At TBD Pharmatech, this standard makes a part of our culture. Every process, from feasibility study to commercial dispatch, is mapped, measured and improved.

Robust change-control and CAPA programs mean lessons travel fast while quality standards keep us audit-ready at all times.

The result is predictable lead times, right-first-time documentation, and a level of reliability that lets clients plan their work with confidence.

Good Manufacturing Practices (GMP) are the guidelines and regulations that govern the manufacturing, testing, and quality assurance of pharmaceuticals, including active pharmaceutical ingredients (APIs), finished dosage forms, and medical devices.

Our facilities operate under current EU cGMP licences, integrating risk-based thinking into every stage of production: qualified suppliers and materials, segregated flows, validated equipment, and real-time environmental monitoring. Batch records are reviewed by independent Quality Assurance before a Qualified Person (QP) releases them, and periodic self-inspections and third-party audits drive continuous refinement. This discipline guarantees lot-to-lot consistency, full traceability, and compliance with authorities’ expectations—delivering the trust our partners and their patients rely on.