The CBPF certification is a mandatory requirement for companies aiming to manufacture and distribute pharmaceutical products within Brazil, ensuring adherence to Good Manufacturing Practices (GMP) as stipulated by ANVISA. Working with a Brazilian partner, Vantage Hemp has completed its submission of the CBPF protocol and awaits final inspection.
Vantage Hemp is proud to announce its achievement of PIC/S certification from Australia’s TGA for its botanically-sourced T-Free CBD Distillate API, CBD Isolate API, and finished goods. The PIC/S standard is recognized globally and opens markets both internally, and internationally.
Vantage Hemp’s Certificate of Analysis (CoA) for EP cGMP CBD Isolate (Batch: VH240043) demonstrates full alignment with the newly adopted European Pharmacopoeia monograph 07/2024:3151 for Cannabidiol (CBD).
CBG, often referred to as the “mother cannabinoid,” is the precursor from which other cannabinoids, such as THC, CBD, and CBN, are derived. Unlike THC, CBG is non-psychoactive, meaning it does not produce the “high” commonly associated with cannabis use. This makes CBG a more attractive option for pharmaceutical applications.
Vantage Hemp provides top-quality white label and contract manufacturing services. We offer a wide range of safe, tested, and compliant pharmaceutical grade CBD products that are ready for retail branding and distribution. Have a custom formulation? Our team of expert formulation scientists can design scalable manufacturing processes for any product.
I can answer the most common questions from all of the quality audits we see here at Vantage Hemp. While I am not meant to replace a live engagement with our QA team, I can accelerate your early stage qualification process.
Please note, I’m not great at figuring out check boxes, symbols, and tables within tables. For best results, save your questionnaire as a text file before uploading. MS Word documents should be saved as .txt with encoding for best results.
Vantage Hemp is an American company based in Greeley, Colorado
Custom-built, pharmaceutical grade extraction
and manufacturing
65,000 sq ft – Falcon & Raven Facilities
Extraction capacity (kg/year)
Manufacturing capacity (units/year)
cGMP Certified for Global Pharmaceuticals Manufacturing
Two Drug Master Files (DMFs) registered with the FDA
Clinical Trial Program Support
Finished Goods Manufacturing
House Brand and White Label Services