Impurities Testing

Ensuring the Purity and Safety of Your Pharmaceutical Products

Impurities testing and contaminant investigations

In the pharmaceutical industry, it is crucial to identify and characterize impurities present in drug substances or products. 

Profarma team of experts understands the importance of method development and validation in impurities testing, and our team is experienced in developing robust methods specific to the impurities of interest.

We offer stability testing services to assess the behavior of impurities over time and under different storage conditions. This helps to ensure the long-term stability and quality of the pharmaceutical products.

At Profarma, we take a customer-oriented approach, tailoring our services to meet the specific needs of our clients. Our testing team is dedicated to providing reliable and timely results, assisting clients in meeting regulatory requirements and ensuring product safety and efficacy.

Frequently Asked Questions

Impurities testing involves identifying and quantifying unwanted chemicals or substances within a pharmaceutical product. These impurities can arise from raw materials, manufacturing processes, degradation, or storage conditions.

Profarma employs advanced analytical techniques such as:

  • High-Performance Liquid Chromatography (HPLC)
  • Gas Chromatography (GC)
  • UV-Vis Spectroscopy

These techniques allow us to accurately identify and quantify impurities in pharmaceutical products.

Yes, Profarma can develop and validate custom impurities testing methods tailored to specific product needs. Our team works closely with clients to create robust testing protocols that meet all regulatory and quality requirements.

Profarma can test a wide range of pharmaceutical products, including:

  • Small molecule drugs
  • Biologics and biosimilars
  • Injectables
  • Topical formulations
  • Inhalation products