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1. Capecitabine (500 mg) Film-coated Tablets. The required quantity is 100,000 units.
2. Methylprednisolone (40 mg) Powder for Solution for Injections. The required quantity is 50,000 units.
3. Dabrafenib (75 mg) Hard Capsules. The required quantity is 43,200 units.
4. Metamizole Sodium (500 mg/ ml in 2 ml) Solution for Injections. The required quantity is 30,000 units.
gaurav@cdymax.in
we can help you with onco api and onco formulation from our USFDA approved facility at bangalore india
gaurav@cdymax.in
we can help you with onco api and onco formulation from our USFDA approved facility at bangalore india
chowdary@carbontree.in
Dear Sir,
We do supply Capacitabine 500mg from our EUGMP facility with BE studies
Regards
PA Chowdary
dep5@techemi.com
Anhui Sinotech industrial co.,ltd one of the leading manufacturer, suppliers of API, Vet.-APIs,.We supply the APIS and documents. The goods is origin China .We can supply the COA and the goods package.. Please contact us : Xu ping
Anhui Sinotech Industrial Co.,Ltd
Tel: 86-551-65692531
Whatsapp/Mob: 0086-13866721542
Email: dep5@techemi.com
Web: http://www.techemi.com
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
sales@winergy.in
We can get you everything available in ready form. We are FDA approved, ISO, WHO, GMP, HACCP & have everything available. Reach out to us over email/whatsapp for further details to help close the order!
