A Celebratory Message from TBD Pharmatech’s CEO.

“The Välja facility in Tartu marks a major step forward for TBD Pharmatech. Purpose-built for high-quality development and GMP manufacturing. We partner with you to move medicines from concept to clinic and beyond.”

Andrus Tasa, PhD

CEO OF TBD PHARMATECH

Announcements

Key Milestones – From Construction to GMP Certification

  • 15.02.2024 Construction Kick-Off - Ground is broken and building work begins on the Välja manufacturing hub.
  • 05.04.2024 – Cornerstone Event - Foundation stone laid at a public ceremony, marking the official start of the project’s rise.
  • 01.12.2024 – Construction Completed - Building shell and utilities hand over.
  • 10.01.2025 – Occupancy Permits Issued - Local municipality grants the occupancy permit.
  • 17.05.2025 – Activity Licence Granted - Estonian Agency of Medicines issues the Activity Permit, authorising pharma operations.
  • October 2025 – GMP audit successfully completed at the Välja site by the Estonian Agency of Medicines.
  • 13 February 2026 – Certificate of GMP Compliance (Manufacturer Authorization) issued for the Välja site by the Estonian Agency of Medicines.
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Core Capabilities

  • 3 000 m² GMP Footprint + 10 Production Suites - Modular design allows rapid re-configuration and future expansion.
  • Expansion opportunities - On-site land reserved for future expansions and additional manufacturing capacity.
  • Multi-Purpose Reactors (50 L – 1 000 L) - Glass-lined and stainless-steel vessels rated from -80 °C to +200 °C for diverse small-molecule chemistries.
  • End-to-End Solids-Processing - Integrated filtration, high-performance centrifugation, and vacuum drying systems work seamlessly with advanced process controls to isolate, wash, and dry complex compounds, delivering low-residual-solvent APIs ready for downstream processing.
  • Precision Process Control & Utilities - Automated temperature, pressure, and inert-gas systems provide reproducible, right-first-time results.
  • Scalability & Tech-Transfer Support - Experienced engineering and quality teams streamline scale-up from lab grams to multi-kilogram commercial campaigns.
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Step Inside. See the Difference.

  • Book Your Visit
    Start the conversation and experience the facility firsthand.

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  • Explore Our Manufacturing Environment
    Tour the Välja GMP site and our Tiigi development laboratories.

Facilities

  • Meet the Experts Delivering Your Project
    Connect with the scientists, engineers, and quality specialists behind every milestone.

About Us

  • Define Your Development & Manufacturing Path
    Walk away with a clear, realistic roadmap tailored to your molecule and regulatory goals.

Services

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