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1. Eltrombopag (25 mg) Film Coated Tablets. The required quantity is 20,000 units.
2. Dexamethasone (4 mg) Solution for Injections. The required quantity is 50,000 units.
3. Temozolomide (100 mg) Capsules. The required quantity is 10,000 units.
4. Capecitabine (500 mg) Film Coated Tablets. The required quantity is 35,000 units.
Comments :
chowdary@carbontree.in
Dear Sir,
We have exclusive Oncology FDF manufacturing facility with EUGMP, Korean GMP, WHOGMP, PICs approvals, MHRA, Belarus and other international accreditations.
We are producing more than 300 products and most of the products available eCTD dossiers.
We do supply below products from our EUGMP Site.
1.Eltrombopag (25 mg) Film Coated Tablets. The required quantity is 20,000 units.
2. Temozolomide (100 mg) Capsules. The required quantity is 10,000 units.
3. Capecitabine (500 mg) Film Coated Tablets.
5000-25000 boxes.
We have manufacturing license for all above products. Please visit our website for more information
Regards
PA Chowdary
bd@spaccurelabs.com
www.spaccurelabs.com
www.tizig.com
We are siyahi traders from India and we can supply this material kindly mention the needed quantity to give sample for analysis that is MOQ. we have ready stock of mentioned products
always as we are purchasing from largest manufacturing unit. Contact us with confidence for more details like COA and GMP with immediate response.
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
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
