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1. Dolutegravir Sodium API
2. Doripenem API
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info@indeximinternational.com
INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED
sales6@iffect.com.cn
Greetings from Iffect Chemphar Co., Ltd!
IFFECT CHEMPHAR CO., LTD. is one of the biggest R&D and manufacturer base specialized in new and high valued added APIs in China, we are both manufacturer and exporter for Pharmaceuticals & Veterinary API and its main intermediates. And now we are on the way to apply for COS and FDA approval for some of our products. Meanwhile we are also willing to register our products in your market if it's requested.
We could supply Dolutegravir sodium at commercial quantity.
More information needed, please feel free to contact.
info@aeqpharma.com
hi,Dolutegravir Sodium and Doripenem APIs in our list,
we can support for all required docs.
info@eqpharma.com
harshad.solanki@apotheconpharma.com
"Greetings for the day !
I take this opportunity to write to you with introduction of Apothecon Pharmaceuticals P. Ltd.
Apothecon Pharmaceuticals established in year 2007 and Apothecon have valid approval like US-FDA, UK-MHRA, Anvisa, TGA, WHO-GMP Etc.
Apothecon offer API, Intermediates and FDF products from Regulatory approved plant.
"
hostrinlifesciences@gmail.com
Dear friend,
Greetings from Hostrin Life Sciences!!!
We have been supporting the following services.
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, 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 software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.
3. Impurity's & Reference standards support for API's
4. Services for IPR & Regulatory compliance
5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.
9. Pharmacovigilance services.
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
priya@mangalamdrugs.com
Dear Team Pharmacompass,
Please share the buyer details.
Regards,
Priya Singh
