Reply
1. PEG 3350 (300 MT - 400 MT) Excipient
2. Ascorbic Acid (10 MT - 20 MT) Excipient
3. Sodium Sulfate (25 MT - 35 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
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE
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
manickt@aamangeniushealthcare.co.in
HI
We are from Nottingham at Beeston NG92QY, supply regularly to EU various excipients like Citric acid anhydrous EMPROVE bio EP BP JP
100
Sodium citrate dihydrate 1.06446
200
Primogel - Sodium starch glycolate [EP/USP]
1,492.11
Microcrystalline cellulose
500
Magnesium stearate
10
Magnesium stearate
300
Magnesium stearate Ligamed MF-2-V
1,000
Microcrystalline cellulose Vivapur 101
4,000
Corn starch Extra white
6,500
Sodium carmellose
Plz send me mail to Citric acid anhydrous EMPROVE bio EP BP JP
100
Sodium citrate dihydrate 1.06446
200
Primogel - Sodium starch glycolate [EP/USP]
1,492.11
Microcrystalline cellulose
500
Magnesium stearate
10
Magnesium stearate
300
Magnesium stearate Ligamed MF-2-V
1,000
Microcrystalline cellulose Vivapur 101
4,000
.Plz send me mail manickt@aamangeniushealthcare.co.in.
Thanks
MANICK.T
bdevomaar@gmail.com
Dear
Please send the inquiry on below email.
We can support your requierment for the excipients with all documents.
bdevomaar@gmail.com
BR
himali.pawaskar@dksh.com
Hi, Please share this lead
kaushal@newedgeoverseas.com
Please connect
