Reply
1. Acetylsalicylic Acid (75 mg) Tablets. The required quantity is 151,200 units.
2. Valproic Acid (300 mg) Tablets. The required quantity is 64,800 units.
Fiona_fu@jindunmedical.com
This is Fiona from Jin Dun Medical China and glad to send you email.
We are the supplier of Pharmaceutical Intermediates and APIs, which are rigorously tested before reaching the market.
From the moment of our establishment we firmly adhere to the philosophy that our success is driven by our customer's success.We work hard to develop a deep understanding of our customers'commercial ambitions in order to engineer the right product for our commercial partners.
www.jindun-medical.com
chowdary@carbontree.in
Dear Sir,
We can supply below products in 3-4 weeks from date of order confirmation with dossier.
1. Acetylsalicylic Acid (75 mg) Tablets. The required quantity is 151,200 units.
2. Valproic Acid (300 mg) Tablets. The required quantity is 64,800 units.
Regards
PA Chowdary
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life Sciences!!!
Hostrin offers 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.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance
5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.
6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) 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
