Pharmaceutical Grade CBD & CBG
At Vantage Hemp, we understand the regulatory process for API registration, Investigational New Drug listings, clinical trial execution, and drug commercialization. With two Drug Master Files registered at the FDA, PIC/S certification from the Therapeutic Goods Administration of Australia. and ICH Q7, WHO GMP, and FDA 21 CFR 210/211 certification from SGS, our extraction and manufacturing facilities are designed to be compliant with all global pharmaceutical standards.
Pharmaceutical Grade CBD and CBG for Global Markets
Vantage Hemp Receives CBPF Protocol Number
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.
Certified PIC/S by the TGA of Australia
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.
EP cGMP CBD Isolate
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).
Announcing Pharmaceutical Grade CBG Isolate
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.
Leading White Label Manufacturing Services
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.
Product Guide 2025
Download Vantage Hemp’s Product Guide 2025 for a complete list of pharmaceutical grade CBD APIs and finished goods.
Compliance Package 2025
Download Vantage Hemp’s Compliance Package 2025 for a complete list of all of our certifications.
ASK VANNA
I’m Vanna, your Pharmaceutical Quality Audit Assistant.
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.
- Ask me any one-off questions from a typical cGMP vendor qualification process
- Let me guide you through a variety of cGMP documentation
- Quality Audit Answer Guide
- cGMP Compliance Package
- Site Master File
- cGMP Quality Manual
- Vantage Hemp Product Guide
- Upload your own Vendor Audit questionnaire and allow me to provide a list of answers.
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.
YOUTUBE: How Pharmaceutical Grade CBD is Made
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)
- CBD Distillate 300,000
- CBD Isolate 200,000
Manufacturing capacity (units/year)
- SoftGel capsules – 50M+
- Tinctures – 1M
cGMP Certified for Global Pharmaceuticals Manufacturing
Two Drug Master Files (DMFs) registered with the FDA
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- CBD Distillate (#036876)
- CBD Isolate (#037784)
Clinical Trial Program Support
Finished Goods Manufacturing
House Brand and White Label Services