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1. Vinorelbine (20 mg) Capsules. The required quantity is 516 units.
2. Carboplatin (150 mg) Injections. The required quantity is 1,155 units.
3. Mitotane (500 mg) Tablets. The required quantity is 600 units.
4. Filgrastim (30 MU/ 0.5 ml) Solution for Injections or Infusions. The required quantity is 1,050 units.
chowdary@carbontree.in
Dear Sir,
We have exclusive Oncology FDF manufacturing facility with W
EUGMP, KOREAN GMP, WHOGMP, PICs approvals, Belarus, MHRA approvals and producing more than 300 products.
We can supply Vinorelbine tablets, Carboplatin&Cisplatin injections and Filgrastim . We have ready stocks 500-1500 vials each product and tablets.
Please visit our website for more information bd@spaccurelabs.com
www.spaccurelabs.com
www.tizig.com
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 )
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
