Reply
1. Kolliphor RH40 (1080 kg) Excipient
2. Macrogol 6000 (150 kg) Excipient
3. Macrogol 400 (3 MT) Excipient
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
bdevomaar@gmail.com
Dear Sir
Please send your inquiry on below email.
We can provide the excipients with COa.
bdevomaar@gmail.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
info@nomismahealthcare.com
Dear,
Greetings from Nomisma Healthcare PVT LTD.
I hope you're doing well...
Nomisma Healthcare brought to you very high-quality bioabsorbable polymers (PLGA, PLA PGA, and its Derivatives) suitable to use as excipients in Drug delivery formulations, Drug-eluting stents, and Bioabsorsable orthopedic implants. All these products are quality certified & designed as per the standard requirements of Nomisma Healthcare.
Please feel free to contact us if any requirements.
niraj@amstermicrocell.com
Please do help me with your email id or contact information.
We are excipients manufacturers based in Ahmedabad, Gujarat, India
www.amstermicrocell.com
