Reply
1. Dolutegravir (10 mg) Dispersible Tablets. The required quantity is 108, 000 units.
2. Dolutegravir (50 mg) Tablets. The required quantity is 180,000 units.
chowdary@carbontree.in
Dear Sir,
We do supply from our WHOGMP& Russian GMP facility
1. Dolutegravir (10 mg) Dispersible Tablets. The required quantity is 108, 000 units.
Lead time. 3-4weeks
2. Dolutegravir (50 mg) Tablets. The required quantity is 180,000 units.
Lead time. 3-4weeks
info@aeqpharma.com
hello we can do pre-mic pellets and FDF.
Thanks
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 APPROVED
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life Sciences!!!
Hostrin offers 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.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance
5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.
6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) 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
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
sunil.kb@medisticsglobal.com
Dear Sir,
Medistics Global Pvt Ltd, 2016 a Star Export House in Merchandise Exports, supply
Active Pharmaceutical Ingredients, Excipients, Essential Oils, Chemicals, Food Additives, Packaging materials Pet and Glass, Print and Packaging, etc.,
We hereby propose to offer a similar service to your organization wherein you will have
a reliable vendor
Sunil
Business Devpt Manager
MEDISTICS GLOBAL Pvt. Ltd.,
#36 ,1 Fl, 11th Cr, Rajajinagar,10
Ph : +91 8147319369
sunil.kb@medisticsglobal.com
inquiry@remedypharma.co.in
We can support the inquiry with best price and dossier. Please connect via email or whatsapp.
