Manufacturing and packaging in comliance with cGMP and ISO 13485
Contract manufacturing of sterile and non sterile, solid, semi solids and lyophilized pharmaceutical products and medical devices
Chemical testing and Analyses, including Biological samples and tissues
Quantitative analysis of pharmaceuticals, natural compounds and metabolites in finished products and biological matrices (including stability programs)
Product development
Development of a wide range of formulations, analytical and bioanalytical methods to achieve an effective dosage form of all types of routes
Manufacturing and packaging in comliance with cGMP and ISO 13485
News
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  • Passover vacation

    Nextar’s team will be on Passover vacation between April 14th until April 21st.  Back at work on April 22nd
  • To free download Nextar's instruction guide for development of drugs

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