Drug Consistency Evaluation

Drug consistency means that the generic drug should be consistent with the quality and efficacy of the original drug, including consistent impurity spectrum, consistent stability, and consistent dissolution law in vivo and in vitro. Although the active ingredients of generic drugs and original drugs are the same, the content of impurities, bioavailability and drug side effects may be different, and the clinical safety and effectiveness of drugs are naturally different. Therefore, drug consistency research must be carried out to improve the safety and effectiveness of drugs and protect human health and life safety.

Drug consistency evaluation has important practical significance. First, drug consistency evaluation can improve the safety and effectiveness of generic drugs to protect the health of patients. Second, drug consistency evaluation helps to promote the development of the pharmaceutical industry, improve the supply of drugs, meet the needs of patients and reduce medical costs.

STEMart provides high-quality drug consistency evaluation services to ensure the safety and effectiveness of generic drugs, reduce medical costs, and promote the development of the pharmaceutical industry.

Test Samples

Generic drugs and small factory drugs

Service Items

• Prescription comparison
• Quality standard testing
• Crystal pattern testing
• Particle size testing
• Impurity testing
• Pharmacokinetic study

For more information about our drug consistency evaluation services, please contact us.