Reply
1. Famotidine (20 mg) Injections. The required quantity is 450,000 units.
2. Omeprazole (40 mg) Injections. The required quantity is 208,800 units.
pharmchem1@ichemie.com
Greetings,
we are a company specializing in exporting a variety of high-quality APIs.
we will not only provide high-quality and cost-effective APIs, but also provide high-quality after-sales service and technical support.
Looking forward to hearing from you so that we can communicate the details.
Yours sincerely,
David Li
Company: HANGZHOU ICH BIOFARM CO.,LTD.
Address: 1306, A Block, Dragon Times Center, 18 WanTang Road, Hangzhou, China
P.C: 310013
Tel: 0086-571-86693576
E-mail: pharmchem1
chowdary@carbontree.in
We do supply from our WHOGMP/EUGMP facility with eCTD dossiers
Famotidine (20 mg) Injections. The required quantity is 450,000 units.
Lead time. 3-4weeks
2. Omeprazole (40 mg) Injections. The required quantity is 208,800 units.
Lead time. 3-4weeks
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
