Contact Us
Contact Us

Analytical Method Development and Validation for Small Molecule Testing

Method Development

Precision in Pharmaceutical Method Validation
Ensuring Analytical Method Validation for Regulatory Compliance

  • Develops methods with the end use in mind. Develops QC friendly methods or uniquely designed methods for a specific purpose.
  • Applies ICH Q14 and USP <1220> to our method development processes for compliance with current guidelines. 

“Portrett Pharmaceuticals executed multiple critical-path method development projects simultaneously
on time and within budget, all with successful outcomes” – Boston Area Pharma Company

Accelerate your drug development with Portrett Pharmaceuticals’ small molecule testing services. With expertise in stability testing, method development, impurity analysis, and filing compliance, we deliver FDA ready, cGMP compliant analytical solutions with rapid turnaround times to keep your programs on track.

5598 Marvin K Moss Lane
Suite 2005
Wilmington, NC 28409
(252) 375-5187
Facebook-f Linkedin

Get Started

What We Do

  • We amplify your program to the next level by tapping into available technology and innovative ideas while standing on an excellent quality foundation.

Downloads