Gemcitabine Pharmaceutical Reference Standards

Aligns Pharma science supply high-quality impurities reference standards of Gemcitabine, pharmacopeial and non-pharmacopeial Gemcitabine impurities, metabolites, stable isotope products, and nitrosamines (N-NO products). Gemcitabine impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

Gemcitabine Hydrochloride is a nucleoside analog used as chemotherapy. It is marketed as Gemzar® by Eli Lilly and Company. Gemcitabine is used in various carcinomas: non-small cell lung cancer, pancreatic cancer, bladder cancer and breast cancer.

Our Gemcitabine impurities reference standard offering includes

• Gemcitabine related products are thoroughly characterized with NMR, MASS, IR and HPLC/ GC purity.
• Gemcitabine products are supplied with detailed COA & analytical data meeting regulatory compliance.
• We can also provide Gemcitabine EP/USP traceable standards based on your requirements.
• The supplied Gemcitabine related products are re-tested at regular intervals.