We’ve been in the Biopharma industry since the early 1990s. As such, we’ve witnessed and participated in just about every aspect of late stage clinical process development, process automation, facility design, build out, and commissioning, pre clinical, clinical, marketed, and marketed revision, scale up, and up/down stream product manufacturing. We’ve converted facilities from paper batch records to EBR, amongst many other paper to electronic system conversions from documents to supply chain, and lab testing. If its been done before- we’ve probobaly done it. If its a new concept- we’re right at home pioneering with the best.
At CTMA, we finish what we start, show up when we’re expected, and do what needs to get done. Note: we will ask you for your feedback to make sure we are delivering the kind of professional service and results that you’re counting on.
Efficiency is the name of the game in a busy, fast paced environment. “Measure twice, cut once.”