15 Jul 2025

Reply

EU /BP /USP Grade Omega-3 API needed in United Kingdom [ENA23519]
A company that focuses on the development and manufacturing of various finished formulations is looking for suppliers of Omega-3 API. The required quantity is 20 kg for development and later 10 MT for commercial purposes. The suppliers must support this enquiry with CEP & CoA.

Comments :

info@zyntex.com.tr

Hello

We can offer the product that you are looking for, pls contact us at zyntex.com.tr.

17:27,  15 Jul 2025

vijay@jackrabbit.in

please email us, we can support and offer your competitive pricing.

regards

vijay

10:03,  16 Jul 2025

info.upharma@gmail.com

We at U Pharma, specialize in supplying high-quality APIs, excipients, intermediates and pellets compliance with WHO GMP, ISO & certified international regulatory standards.

We can supply you the subjected API.
Kindly send us your enquiry on info.upharma@gmail.com or info@upharma.org

Check our product list https://www.upharma.org/products

Kind Regards,
Meenaz
U Pharma
Add: Mumbai 410206 India
Whatsapp: +91 8097965160
https://www.upharma.org

12:46,  16 Jul 2025

sibi.gopalsamy@nhgpharma.com

We New Horizon Pharma are Manufacturers of APIs, supplying to global regulatory markets, including the US, EU, LATAM & MENA. With strategic sales offices in 7 locations worldwide, we supply niche and orphan drug APIs. We are equipped with a diversified portfolio of APIs with USDMFs & CEPs manufactured in USFDA/EU GMP compliant facilities. In addition to this, we represent 7 Indian Partner Sites with their portfolio of over 400 APIs.

14:34,  16 Jul 2025

hostrinlifesciences@gmail.com

Hostrin Life Sciences
*One Stop For Pharmaceutical and Biosimilar Regulatory Solutions.

Hostrin offers the following services:

1.Out-licensing Dossiers
2.Dossiers in CTD/ACTD/eCTD formats
3.CDMO (Contract Research & Development)
4.Tech transfer support and Registration of Dossiers in all markets.
5.eCTD publishing with potential softwares and addressing post submission queries from all regulatory authorities.
6.QBD & QMS_Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP Assessment Audits.
7.BE studies and clinical studies from US-FDA, EU-GMP, UK-MHRA, TGA-Australia/GCC/ANVISA approved CRO's/BE Study Centers.
8.Synthetic Resin technologies support.
9.Cleaning validation/ toxicology study reports (PDE/ADE I OEL) values for API's & FDF's
10.Pharmacovigilance

Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
www.hostringlobal.com

00:04,  17 Jul 2025

Cristonelifecare@gmail.com

We will supply your requirements,
Please send your requirements to cristonelifecare@gmail.com
Please visit our website: www.cristoneglobal.com

00:14,  17 Jul 2025
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