11 Aug 2023

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Meldonium Dihydrate API needed in Uzbekistan [ENA17799]
A company that deals in various pharmaceutical products is looking for suppliers of Meldonium Dihydrate API. The initial required quantity is 25 kg for trial & 175 kg for commercial purposes. The suppliers must support this enquiry with DMF, GMP & CoA.

Comments :

vetapi2@aarambhlifescience.com

Please send us inquiry by email

10:59,  11 Aug 2023

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer APIs along with the supporting documents.Kindly let us know your email id so that we can send you the email and we can give you the best price.

Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA

11:21,  11 Aug 2023

crystalchemicalsfzllc@gmail.com

Crystal Chemicals FZ LLC is a supplier & Distributor of Active Pharmaceutical Ingredients (API’s) in Dubai, United Arab Emirates (UAE)

We can supply the following API, please contact

CRYSTAL CHEMICALS FZ-LLC
(Pharmaceuticals API's Distribution House in UAE)
Mobile & (Whatsapp) +971542360830
Email: crystalchemicalsfzllc@gmail.com
Website: www.crystalchemicals.ae

13:39,  11 Aug 2023

hostrinlifesciences@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.

Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.

2. eCTD publishing with potential softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance with all risk assessments.

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. Pharmacovigilance services.

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

For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com

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

01:46,  12 Aug 2023

info@shreechemicalsimpex.com

Hello,
We, "SHREE CHEMICALS IMPEX " are contract manufacturer, supplier and exporter of active pharmaceutical ingredient, pharmaceutical intermediate and agrochemicals.
We can fulfill your requirements.
Please contact on following details.
E-mail : info@shreechemicalsimpex.com
Mo-no : (+91) 8200048670

13:10,  12 Aug 2023

nicole.deng@chsdpharma.com

Direct manufacturer with CEP support.
Please drop email at nicole.deng@chsdpharma.com

13:55,  15 Aug 2023
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