Quality and manufacturing

From the moment research and development begins to the time our medicines reach patients, Teva’s commitment to quality is uncompromising

Teva's extensive global operations network includes approximately 21,000 employees at more than 50 manufacturing facilities in 33 countries 01.

Here in Ireland, we have two main locations in the Republic of Ireland and one in Northern Ireland. 

  • We have a large manufacturing site in Waterford which focuses on the manufacture and development of respiratory products and devices for supply to the United States and around 30 other global markets. It includes an onsite research and development centre.
  • We have a Commercial / Support office in Swords, near Dublin.
  • In Northern Ireland, we have research and development facilities in Larne
Learn more about Teva in Ireland

 

We strive to deliver quality generic and specialty medicines to different markets - quickly and effectively. The team that makes this happen spans several areas of our business including Research & Development, Quality Assurance, Regulatory Affairs, scientific and logistical support, customer service, marketing and sales.

Quality Assurance

Teva’s commitment to quality is uncompromising and we manufacture according to the highest quality and compliance standards. This focus is evident at every stage of the development and production of our medicines.

All of our manufacturing processes are validated and products are tested and certified, using state-of-the-art testing equipment throughout the manufacturing process that ensures adherence to the highest quality and compliance standards.

Teva Global Operations is dedicated to optimising the performance of our global supply chain from the time we procure our first raw materials to the moment our medicines reach patients.

We know that a timely, reliable and cost-effective global distribution capability is critical to providing customers and patients with effective, high-quality products where and when they need them. Our high-volume, technologically-advanced distribution facilities allow us to deliver best-in-class products swiftly and reliably. 

Teva closely controls product quality and external suppliers, who must meet the same tough requirements we set for ourselves. As a result, we have an enviable record of Current Good Manufacturing Practice (cGMP) compliance, which is assessed by the US Food and Drug Administration (FDA) and other global regulatory organizations.

References

  1. Back to contents.

    Based on Teva Global Operations internal data.


Generic medicines

Generic medicines

We supply a wide range of generic medicines to Irish pharmacies

Learn more

Specialty medicines

We develop and improve treatments for patients across multiple therapy areas

Learn more

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Date of preparation: January 2025
Reference: D: COB-IE-NP-00036 (V4.0) / T: GEN-IE-NP-00134 (V1.0) / M: GEN-IE-NP-00136 (V1.0)