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At Sterling, we combine a full-service offering with expert knowledge and technical agility to offer full-service API development and cGMP contract manufacturing capabilities. We can support your projects through the entire product lifecycle from grams to tonnes.
We pride ourselves on being easy to do business with and we’re dedicated to offering flexible and tailored solutions that suit our customers’ needs. Our 400+ strong team across our facilities in the UK and the US are capable of handling even the most hazardous chemical processes safely. Our industry leading compliance culture and performance is part of our day-to-day work and we work hard to maintain the Sterling standards.
Dedicated to adding value through continuous improvement we are constantly exploring new and improved ways of doing things as part of our technology and innovation programme as we consistently strive to remain leaders in our field.
With over 50 years’ experience our exceptionally talented team combine their unrivalled knowledge with first-class customer service to ensure high quality project delivery, every time.
For more information, please visit www.sterlingpharmasolutions.com.
At our US facility in Cary, North Carolina we deliver expert chemistry solutions for pre-clinical and early phase clinical supply.— Sterling Pharma (@sterling_pharma) July 8, 2020
Join our President of US Operations, Mat Minardi, for an overview of the US facility and the team’s expertise - Watch here: https://t.co/QCUC4JYtzC
Filled with informative content crafted by our expert team, our Sterling hub offers you unique insights into the latest advancements across the drug development and manufacturing life cycle.— Sterling Pharma (@sterling_pharma) July 7, 2020
Sign up to the Sterling Hub here: https://t.co/KrK6WMkrB8