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30.03.2016, admin  
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Each pharmaceutical product undergoes rigid process validation, stability-indicating method validation, and method development protocols during each manufacturing and analytical process. Our manufacturing processes follow the highest standards and our quality assurance and control procedures are stringent. Our adherence to exacting quality assurance and quality control standards assures you that your precise product specifications are consistently met. Nexgen can provide services including: methods development, method validation, stability testing, comparative dissolution testing, as well as raw material, in-process and finished goods analysis.


Gone are the days when the Brand Owner or Own Label Distributor could abdicate the responsibility for the quality of their products to the Contract Manufacturing Organization. We identify raw materials to ensure proper potency and purity using advanced analytical techniques, and formulate to meet DSHEA, and where indicated, USP requirements. Nexgen adheres to the strict standards of the current Good Manufacturing Practices (cGMPs) established by the US Food and Drug Administration, and the Natural Products Association.
With over 30 years of experience in manufacturing dietary supplements, Gemini offers a complete suite of services designed to develop and manufacture a cGMP compliant product for our customers.


The attached link to a whitepaper on Do You Really Know the Quality of Your Dietary Supplements will explain the challenges in today’s market and the value of a partnership program.



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