Reply
please send us inquiry by email please
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
heliantus@heliantus-milano.it
Estimados
Tenemos este producto en llegada a neustro almacen. Si es de su interes, contactarnos a:
marco_sgaravatti@hotmail.com
heliantus@heliantus-milano.it
Saludos cordiales
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
api@caren.se
Please send your full regulatory requirements to our email.
Our international team will be able to look into this for you.
Best Regards,
Ming Yuzhen (Marketing & Sales)
Tel: +8618411631209
Email: api@caren.se
a.izadi@pharmanova.ae
Dear Sir/Madam,
Dear Sir/Madam,
I hope everything is well on your side.
I am Ashkan, Business Development Specialist at PharmaNova. PharmaNova is a wholesaler pharmaceutical raw material company and located in Dubai UAE with branches in Turkey, India and Hong Kong. We are providing top quality pharmaceutical raw material worldwide. We have very good network within China, India and Europe to support our customers worldwide from certified and regulated API and Excipients manufacturers, audited by international MOHs.
We are able to support you from certified European Source.
Please let me know if you are interested.
Regards
Ashkan Izadi
himali.pawaskar@dksh.com
Hi, Please share this lead
