At the core of our pharmaceutical manufacturing is a robust quality system built for global compliance and client trust. Our team of experienced quality professionals ensures every product is developed and manufactured in accordance with current Good Manufacturing Practice (cGMP) and ISO 9001 standards.
Our Tiigi facility in Tartu Biotechnology Park serves as the operational nucleus, hosting:
Our new Välja facility will expand our GMP capacity with:
ASMF, DMFs, CEPs as per customer need
Our ISO 9001:2015-certified Quality Management System is integral to TBD Pharmatech’s daily operations, guiding work from early R&D through GMP batch release. Every workflow is formally mapped, routinely measured, and subject to scheduled reviews so that process performance and compliance remain transparent and traceable.
A dedicated Quality Assurance team carries out rolling internal audits, management reviews, and real-time deviation tracking to maintain constant inspection readiness. Structured change-control and CAPA programmes capture lessons learned and translate them into documented process improvements, while supplier qualifications, audits and client feedback provide the data needed for ongoing system updates.
These measures deliver predictable lead times, accurate documentation, and consistent product quality across both the Tiigi and Välja sites, supporting reliable project planning and regulatory compliance.
API CDMO that delivers a tailored range of fine chemical development and manufacturing solutions to pharmaceutical and biotech companies.
