Some people dream of success. We make it happen

Quality control

Our team can assist you with numerous routine and specialized analysis:

HPLC, GC and IC analysis

  • Active Pharmaceutical Ingredients (API)
  • Residual solvents
  • Heavy metals
  • Vitamin assays
  • Protein/Nitrogen analysis
  • Pesiticides
  • Physical and wet chemical analysis
  • Total organic carbon (TOC)
  • Dissolution studies
  • Spectroscopy

Stability Services

Our stability services include:

  • 25°C/60% RH (ICH zone I and II conditions)
  • 30°C/65% RH (ICH zone IV a conditions)
  • 30°C/75% RH (ICH zone IV b conditions)
  • 40°C/75% RH (Accelerated stability)

    All chambers are fully mapped, qualified, controlled and 24/7 monitored with alarm system.

  • In-use stability studies to simulate patient use    of drug product
  • Storage available for short and long term durations, alone or with analyses​​

Method development & validation services

At ILS Pharma methods are validated according to current ICH guide lines and client’s requirements for:

  • Determining the dosage of active ingredients in raw materials and finished products
  • Degradation studies
    Dissolution studies for all types of solid dosage forms
  • Dissolution studies for all types of solid dosage forms

We perform technological transfers of existing methods from other laboratories and also provide verifications of Pharmacopeias.
Stability Services