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1. Paclitaxel (100 mg) Powder for Dispersion for Infusions. The required quantity is 190,000 units.
2. Imatinib (100 mg) Film Coated Tablets. The required quantity is 1,360,800 units.
chowdary@carbontree.in
Dear Sir,
We have exclusive Oncology FDF manufacturing facility with EUGMP, MHRA, Korean GMP, WHOGMP, PICs approvals, Belarus GMP, Mexico and many other accreditations.
We can able to supply Paclitaxel 100mg powder and Imatinib 100mg tablets before target date.
We have eCTD dossiers for 200 products
Please visit our website for more information
Regards
PA Chowdary
bd@spaccurelabs.com
www.spaccurelabs.COA
Hyderabad, India
chowdary@carbontree.in
Dear Sir,
We have exclusive Oncology FDF manufacturing facility with EUGMP, MHRA, Korean GMP, WHOGMP, PICs approvals, Belarus GMP, Mexico and many other accreditations.
We can able to supply Paclitaxel 100mg powder and Imatinib 100mg tablets before target date.
We have eCTD dossiers for 200 products
Please visit our website for more information
Regards
PA Chowdary
bd@spaccurelabs.com
www.spaccurelabs.com
Hyderabad, India
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers and it can be available with us.
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 )
info@aeqpharma.com
We can partecipate to tender with Eu registered products.
Contact us for get our best quote
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
