Pharmaceuticals and Scientech Labs

The US pharmaceutical industry is one of the most highly regulated industries in the world. Scientech’s Quality Program assures the accuracy and cGMP compliance of all data and results.

Scientech partners with manufacturers, raw material suppliers, and formulators during each stage of the drug development process to assist with pharmaceutical and chemical analysis.

  • Method Development and Validation in 3-4 Weeks (expedited TAT available)
  • Finished Product & Release Testing in 3-5 Days (expedited TAT available)
  • Stability Programs (real time, accelerated, Zone IVa, Zone IVb)
  • Vendor Qualifications for Active Pharmaceutical Ingredients (APIs), Raw Materials, Solvents, Excipients, and Other Process Reagents
  • Cleaning and Process Validation
  • Method Transfer
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cGMP

cGMP compliant

FDA

FDA registered

DEA

DEA licensed

SOPs

Documentation