29 Feb

Posted at 00:35h in Latest News, News, Pharmaceutical by
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[vc_row css_animation="" row_type="row" use_row_as_full_screen_section="no" type="full_width" angled_section="no" text_align="left" background_image_as_pattern="without_pattern"][vc_column][vc_column_text css=""] US producer reaffirms leadership position through recent regulatory milestone  Greeley, Colorado – Vantage Hemp Co. (“Vantage” or “the Company”), a globally accredited plant-based extractor and finished product manufacturer, is proud to announce that it has successfully obtained Good...

21 Sep

Posted at 03:05h in News, Pharmaceutical by
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Leading producer’s compliance with stringent regulatory requirements drives global expansion Greeley, Colorado, September 21, 2023 - Vantage Hemp Co. (“Vantage” or the “Company”) announces the completion of a rigorous four-day audit conducted by Australia's Therapeutic Goods Administration (TGA), the country’s government authority responsible for evaluating, assessing,...

03 Apr

Posted at 19:36h in Latest News, News, Pharmaceutical by
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[vc_row][vc_column][vc_column_text] Leading producer reinforces its commitment to bringing the highest quality ingredients to clinical trials and the food additive, dietary supplement, and pharmaceutical industries Greeley, Colorado, April 4, 2023 - Vantage Hemp Co. (“Vantage” or the “Company”) announces that it has submitted a Drug Master File (DMF)...

24 Aug

Posted at 13:08h in Blog, Food Ingredients, Natural Health Products, Pharmaceutical by
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CBD - Transparency & Regulation for Consumer Safety CBD (cannabidiol), one of many cannabinoids derived from the plant Cannabis sativa L. (cannabis), has gained great popularity among consumers in recent years. The exponential growth of CBD in all consumer product categories might be taken to suggest...

01 Jul

Posted at 08:29h in Blog by
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To explain what exactly it means to have Good Manufacturing Practices (GMP) is to ensure the consistent quality and safety of products by focusing on five key elements, which are often referred to as the 5 P's of GMP—people, premises, processes, products and procedures. GMP describes the minimum standard that a medicines manufacturer must meet in their production processes. The European Medicines Agency (EMA) coordinates inspections to verify compliance with these standards and plays a key role in harmonizing GMP activities at European Union (EU) level.