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1. Fulvestrant (250 mg) Solution for Injection in Pre-filled Syringes. The required quantity is 7,448 units.
2. Rituximab (500 mg) Injections. The required quantity is 6,648 units.
chowdary@carbontree.in
Dear Sir,
We can supply captioned products from our WHOGMP/EUGMP facility
We are producing Adalimumab, Bevasizumab, Cetuximab, Rituximab, Trastuzumab, Pembrolizumab, Nivulomab, Darbepoetin Alfa B and Teriparatide from WHOGMP facility.
1. Fulvestrant (250 mg) Solution for Injection in Pre-filled Syringes. The required quantity is 7,448 units.
Lead time. 4-5weeks
2. Rituximab (500 mg) Injections. The required quantity is 6,648 units.
Ready stocks. 3500 units & 3148 units in 30-45days
COA, Artwork, COPP/FSC, Packinsert & WHOGMP will be submit along with the quote.
Best Regards
PA Chowdary
arunodayalabs@gmail.com
hoventapharma@gmail.com
Dear sir/madam,
We would like to take this opportunity to Introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement
hoventapharma@gmail.com
Dear sir/madam,
We would like to take this opportunity to Introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement
hoventapharma@gmail.com
Dear sir/madam,
We would like to take this opportunity to Introduce Hoventa Pharma,
We offer various kinds of services in addition to supplies of APIs,and intermediate, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement
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
