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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
SALVAVIDAS PHARMACEUTICAL PVT.LTD
We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.
We deal with Finish Products, Surgical items. We also Deal with Branded Drugs along with all Related Documents and Certificates.
We are also dealing in Active Pharmaceutical Ingredients (API’s), Intermediates, Excipients & Chemicals…
We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.
If you have any requirements, doubts or queries then feel free to contact us.
We are always there to serve you with our best services
All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.
All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.
Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com
info@grefuel.com
Dear Sir/Madam,
Greetings from Grefuel Private Limited...!!
Hope you are doing well.
We are one of the leading manufacturer, supplier and exporter of Pharmaceutical bulk drug and its Intermediates & Chemicals in India. If you have any requirement for the same, please send us your valuable email on info@grefuel.com We will be pleased to offer you our competitive prices with prompt delivery.
Our manufacturing plant as per GMP guidelines which itself shows our commitment to strict quality standards set by National & International Regulatory compliances.
Looking forward to a new business relationship with you.
Thanks & Regards
Pratik Patel
Grefuel Private Limited
F-14, Lakeview Plaza, Opp. GIDC Lake,
GIDC, Ankleshwar, Bharuch, Gujarat,
India - 393 002
Mob. +91 91731 91981 (WhatsApp)
chowdary@carbontree.in
We can supply Iopromide from GMP certified facility
sales1@jnchsd.com
Dear Sir/Madam:
Greetings of the day. We are The Manuafacturer’s of API and Intermediates.
We, Shandong Chenghui Shuangda Pharmaceutical Co.,Ltd, are cGMP plant who manufacrtures the APIs and intermediates. Some of our major products are mentioned below:
Vonoprazan Fumarate
LeterMovir
Dapagliflozin
Crisaborole
Sugammadex
Ropivacaine HCI
Tetracaine HCI
Tetracaine
Prilocaine
Lidocaine
Ozagrel Sodium
Celecoxib
Pramoxine HCI
Meldonium
We could supply above APIs and their main intermediates. If you are intrested in any of them,please feel free to contact me by sales1@jnchsd.com Tel:86-531-58897062,
Fiona
heliantus@heliantus-milano.it
Dear Sirs,
We can offer you said API. Can you contact HELIANTUS SRL, in Italy.
Our mail are:
marco_sgaravatti@hotmail.com
heliantus@heliantus-milano.it
Thank you & bst regards
Marco
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
