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About Us

Quality control analyst

About TBD Pharmatech

Pharmaceutical API CDMO

Specializing in the development and manufacturing of Active Pharmaceutical Ingredients (APIs) and other fine chemicals, TBD Pharmatech (formerly known as TBD-Biodiscovery) stands as a Contract Development and Manufacturing Organization (CDMO) with an established industry presence since 2006. We leverage our robust R&D capabilities and GMP-compliant manufacturing facilities (since 2008), including a state-of-the-art plant currently in construction in Tartu, Estonia.

Located within the European Union and ISO 9001 certified, our international team is devoted to forging lasting connections with our global customer base. International projects account for ~95% of our portfolio—we are adept at navigating complex regulatory landscapes all over the world.

Our tailored suite of services encompasses every stage of chemical development, making us your ideal partner for transforming innovative concepts into commercially viable products. Our commitment to quality and customer satisfaction is affirmed by enduring client relationships: around 80% of our business is generated from returning customers.

Meet the team

Certifications

ISO 9001

ISO 9001:2015 is a globally recognized standard for quality management systems (QMS). Developed by the International Organization for Standardization (ISO), it sets the framework for the processes, procedures, and responsibilities required to achieve consistent product quality focusing on client satisfaction, risk management, and continuous improvement.

Organizations that attain this certification have demonstrated their capability to consistently deliver products or services that meet client and regulatory requirements.

Good Manufacturing Practice (GMP)

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.

GMP compliance ensures that products are consistently produced and controlled according to quality standards and are safe and effective for their intended use. The guidelines encompass everything from raw material sourcing and production facility design to personnel training and record-keeping.

Facilities

TBD’s current site including R&D labs, GMP compliant manufacturing areas and support staff areas are in Tartu Biotechnology Park, Tartu, Estonia.

Currently, TBD is planning an expansion and is in process of constructing a new complex for development and production that significantly expands the available operational capacities.

Facilities

Timeline

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