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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  • Summer vacation

    Nextar’s team will be on summer vacation between August 24  until August 28.  Back at work on August 31 .
  • To free download Nextar's instruction guide for development of drugs

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