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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
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE
info@aeqpharma.com
Ketoprofen Api supply with support docs
sam.d@micoson.com
USD;80/KG CIF sam.d@micoson.com
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
bdevomaar@gmail.com
Dear Sir
Please send the inquiry on below email.
We can support your requierment for the API with all documents.
bdevomaar@gmail.com
Kind regards
chowdary@carbontree.in
Dear Sir,
We do supply Ketoprofen with USDMF from WHOGMP certified facility
tianranbiotechz@gmail.com
Our company is located in Uganda, Africa. The factory directly supplies medical bovine skin gelatin, which is suitable for capsules, soft gel, etc. welcome to negotiate and cooperate
tianranbiotechz@gmail.com
tianranbiotechz@gmail.com
Our company is located in Uganda, Africa. The factory directly supplies medical bovine skin gelatin, which is suitable for capsules, soft gel, etc. welcome to negotiate and cooperate
tianranbiotechz@gmail.com
yangxiaoqing2@ncpc.biz
NCPC, one of the largest pharmaceutical enterprise in China can meet your requirements. Please send the detailed inquiry to yangxiaoqing2@ncpc.biz.
himali.pawaskar@dksh.com
Hi, Please share this lead
himali.pawaskar@dksh.com
Hi, Please share this lead
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
