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1. Enoxaparin Sodium (40 mg/ 0.4 ml) Injections. The required quantity is 500 units.
2. Povidone-Iodine (45 mg/ ml) Solution. The required quantity is 350 units.
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?
Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )
pei@sunmingpharm.com
Comments :
pei@sunmingpharm.com
Hello
Myself Ammy from China SUNMING PHARMACEUTICAL LIMITED. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?
Please, contact
pei@sunmingpharm.com
nathusalunkhe@gmail.com
Hello,
We,shrutas pahrmaceutical" are contract manufacturer, supplier and exporter of active pharmaceutical ingredient, pharmaceutical intermediate.
We can fulfill your requirements.
Please contact on following details.
nathusalunkhe@gmail.com
Enoxaparin Sodium (40 mg/ 0.4 ml) Injections 400/-Rs
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
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
naishadh@swiss.in
We have EU GMP and can supply all these products. Plz get in touch
naishadh@swiss.in
We have EU GMP and can supply all these products. Plz get in touch
naishadh@swiss.in
We have EU GMP and can supply all these products. Plz get in touch
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers of pharmaceutical products.
can we connect for some business?
Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )
