amine@pioneersgroup.com
Dear Mr/Ms, ?
I hope you are staying safe and healthy!
Many kinds of active Pharmaceutical Ingredients, is there any requirement? If any, please don't hesitate to contact us.
And for more information about our company, visit our website: http://www.pioneersgroup.com/
Looking forward to your kindly reply.
Thanks and Best Regards,
AMINE SABER (Sales Manager)
Pioneers International Trading Ltd.
Mob & Whatsapp: +86 183-6046-2124
Email: amine@pioneersgroup.com
alicechan@huarizy.com
HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.
1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80
email address: alicechan@huarizy.com
phone number: +86 18820220687
tracy@grandpharma.cn
Dear Sir/Madam,
It's very glad to see your inquiry of CBD. We have good offer of this product. Pls feel free to contact us for more details.
Contact: tracy@grandpharma.cn
sales@purechempvtltd.in
Pure Chem Pvt. Ltd. is WHO-GMP certified Active Pharmaceutical Ingredients (APIs) and Advance Drug Intermediates Manufacturing and Exporting Unit, established in 1996, Located in Gujarat, INDIA.
We are exporting many of our products to Latin American countries, and Globally.
Also, most of the products are from WHO cGMP, ISO, GMP manufacturers as well.
Product List: https://purechempvtltd.in/our-products/
Website: https://www.purechempvtltd.in
Email: sales@purechempvtltd.in
Whatsapp: +91-8037431744
nelson.junior@pratidonaduzzi.com.br
We are manufacturer of Cannabidiol pharma grade; our CBD API has the following characteristics:
1. Produced by chemical synthesis, that is, the active ingredient is obtained through chemical reactions that modify the structure of simpler substances, so-called starting materials, until it reaches the active ingredient, 100% identical to the natural;
2. As consequence of its synthetic origin, our CBD is free of Tetrahydrocannabinol (THC), heavy metals, weed killers and pesticides;
3. Quality attributes, residual solvents, elemental impurities and stability study in accordance with the ICH guidelines;
4. Organic impurities (including Delta-9-THC and Delta-8-THC) bellow to 0.06% (complies for 1750 mg maximum daily dose, according to ICH Q3A(R2));
5. DMF prepared in accordance with the M4Q guideline;
6. Fully characterized reference standards of Cannabidiol and its related impurities available;
7. GMP certification from ANVISA (Brazilian Health Authority), member of ICH and PIC\S.
Have you interest in synthetic Cannabidiol API? Please, contact us.
Mr. Nelson Ferreira Claro Junior, Ph.D. – Director of API
nelson.junior@pratidonaduzzi.com.br
www.pratidonaduzzi.com.br
AAmbrosi@Noramco.com
Purisys can provide the Cannabidiol product and support you are requesting.
Leveraging decades of expertise in controlled substance
development, licensing and scale up, Purisys offers
cannabinoid-focused companies a fully integrated supply
chain for synthetic cannabinoid-based APIs.
• A highly reliable supply chain which includes multiple key
raw material suppliers.
• API production facilities in both the United States and
Europe enable us to meet your demand for large-scale
commercial supply and remain compliant with government
agency regulations (e.g. DEA Import/Export rules).
Please call or email me to discuss.
Anthony Ambrosini
VP Commercial Operations
215-350-9795
Email: AAmbrosi@Noramco.com
kevin@averixbio.com
Hello,
Averix Bio has phytocannabinoid API CBD Isolate with a DMF at the US FDA. Our extraction facility is in the USA and can ship directly from our facility. We are the first and only (21 CFR Parts 210/211) cGMP & ICH Q7 cannabinoid extraction facility in the United States with a DMF at the FDA.
Looking forward to working with you and for more information please email, kevin@averixbio.com
Kevin Rudolph
Averix Bio
1-919-432-4548
kevin@averixbio.com
calvin@brainsbio.com
Hi there,
We have EU GMP CBD API from a MHRA approved facility in the UK. Through our wholly-owned subsidiary. BSPG Laboratory, is one of a very limited number of organizations listed on the Eudralex GMP website with an EU-GMP and GDP certificate for CBD which is authorized for use in both human and veterinary medicinal products.
Please let me know if you'd like more information.
Calvin Rasode
Brains Bioceutical Corp
www.brainsbio.com
calvin@brainsbio.com
Hi there,
We have EU GMP CBD API from a MHRA approved facility in the UK. Through our wholly-owned subsidiary. BSPG Laboratory, is one of a very limited number of organizations listed on the Eudralex GMP website with an EU-GMP and GDP certificate for CBD which is authorized for use in both human and veterinary medicinal products.
Please let me know if you'd like more information.
Calvin Rasode
Brains Bioceutical Corp
www.brainsbio.com
calvin@brainsbio.com
Hi there,
We have EU GMP CBD API from a MHRA approved facility in the UK. Through our wholly-owned subsidiary. BSPG Laboratory, is one of a very limited number of organizations listed on the Eudralex GMP website with an EU-GMP and GDP certificate for CBD which is authorized for use in both human and veterinary medicinal products.
Please let me know if you'd like more information.
Calvin Rasode
Brains Bioceutical Corp
www.brainsbio.com
hbowerman@transopharm.com
Transo-Pharm USA is able to supply Cannabidiol API to this US customer. Please put in touch with this customer
hbowerman@transopharm.com
Transo-Pharm USA is able to provide hemp based CBD API with the following:
- Current commercial scale 80 MT annually
- Pharmaceutical Grade 99.5 % assay
- THC controlled to < 0.1%
- total impurities < ICH limits
- DMF will be filed OCT 2022
- samples now available