With over 3000 customer-centric employees, operations and commercial offices across the US, EU and China, Porton Pharma Solutions provides global pharmaceutical companies with innovative, reliable and end-to-end process R&D and manufacturing services across small molecule APIs, dosage forms and biologics.
Our Process Technology Centers and WHO/USFDA/EMA/PDMA/NMPA-inspected Manufacturing Facilities feature state-of-the-art equipment, highly flexible cGMP-compliant production assets, plus over 1200 highly skilled scientists and process engineers, all backed by a proven program management system dedicated to seamlessly delivering successful outcomes for your unique project requirements.
We are committed to be the most open, innovative and reliable pharmaceutical service platform in the world and Enabling public’s early access to good medicines. We constantly strive for excellence, and have been recognized through awards by industry forums and global pharmaceutical companies for our process innovation, supply chain performance and compliance with global Quality and EHS standards. By efficiently advancing development and enabling commercialization of multiple high-impact medicines, Porton is proud to have earned the trust of some of the world’s leading and most innovative pharmaceutical companies and many biotechnology companies across the US, EU and Asia.
USD489Million
50%+
4000
5
> 300
> 80
2021 Revenues
yoy (Revenues)
Employees
Regulatory Inspections of USFDA, PMDA, EMA and NMPA
Global Client QA Audits
Global Client EHS Audits
We are committed to helping our global customers efficiently develop high-impact and life-saving medicines, while sustainably and ethically building our business. Our social responsibility philosophy is Enabling public’s early access to good medicines; ensuring the health and well-being of our employees and communities; and emphasizing ethics and transparency in our dealings with all stakeholders.
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