Our analytical R&D team and Quality control team supports all stages of pharmaceutical development including:
- Method development and validation services for wide range products using analytical technologies, such as UPLC, Arc HPLC, LCMS, etc.
- Preparing complete specifications for raw materials, API’s, finished products, intermediates and excipients
- Conducting in-house tests for strict control of pharmacopeial materials and products,
- Conducting stability studies of APIs and formulations in accordance with applicable guidelines,
- Analyzing active ingredients and key raw materials.
- Screening of API’s and formulations for genetoxic impurities such as NDMA/ NDEA.