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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 APPROVE
naresh.kiri@sumarbiotech.com
Drool mail
info@aeqpharma.com
Mupirocin API with full support docs available on our list.
DMF,CEP/COS,EDQM..est..
excellentpharmachemi@gmail.com
Dear Sir,
We will support you for 10kg Mupirocin , kindly send you inquiry on below mail ID.
Regards,
Excellent Pharmachemi LLP
crystalchemicalsfzllc@gmail.com
We have good price of Mupirocin along with DMF Support, Please contact me at
Thanks and Regards,
Dr. Amna Nawaz
CRYSTAL CHEMICALS FZ-LLC - ( India | China | Pakistan | UAE )
M: +92-321-8444610 (Whatsapp)
Skype: Crystalchemicals786
E: import@crystalchemicals.com.pk, crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk
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
sales2@comhony.com
Dear Sir,
Greetings from Shawn Liu in Fujian Comhony Biotechnology Co., Ltd in China.
As a qualified manufacturer, we are producing Mupirocin USP/EP/BP in our GMP-approved facility.
Drop me an email at sales2@comhony.com for more details and the latest quotation!
Cheers!
Shawn Liu
Regional manager
Fujian Comhony Biotechnology Co., Ltd.
