You’re low on time or resources, particularly when you need a specific instrument for a specific job. As not all instruments can do any test, you need a specific test that requires a specific instrument with a validated method that can give quality results. This is what gets your drug to market. Small company, big company, doesn’t matter – you don’t want or need the hassle of knowing every little thing about every single procedure and gaining verification for that device, particularly when the device alone will break your budget. You really just want the needed information to provide data to the FDA to get your latest development to market and keep it there with as few issues as possible.
PTL is a proven cGMP compliant laboratory, in accordance with 21 CFR, Part 210, 211, and Part 11. Our facility is FDA registered and inspected, and we host over 30 audits per year from the world's largest pharmaceutical companies. While the way we interact with colleagues and clients has changed due to recent social distance guidelines, the need for audits has not.
