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1. Flucytosine (250 kg)
2. 1,2,3-Triacetyl-5-deoxy-D-ribose (500 kg)
3. Pentyl Chloroformate (500 kg)
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life sciences!!!
We have been supporting for the following services.
1.We do support DMF's for API's, Tech transfer support and Registration of Dossiers in ROW/MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.
2. Impurity's & Reference standards support for API's
3. Services for IPR & Regulatory compliance
4. 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.
5. Custom synthesis & Contract manufacturing services
6. Synthetic Resins technologies support
Pls don't hesitate to send your enquiry's. For your reference please go through our website www.hostringlobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
navee@chemyzolab.com
Sir kindly contact for anticancer intermediates,i hope your into capecitabine API ,We offer you capecitabine intermediate, we can supply Gemcitabine intermediate also drop mail to me we take custom manufacturing new query molecules and reported pharma intermediates and speciality chemicals contact us navee@chemyzolab.com
navee@chemyzolab.com
Sir kindly contact for anticancer intermediates,i hope your into capecitabine API ,We offer you capecitabine intermediate, we can supply Gemcitabine intermediate also drop mail to me we take custom manufacturing new query molecules and reported pharma intermediates and speciality chemicals contact us navee@chemyzolab.com
rkdpm84@gmail.com
we are ready to supply
chaitanya@solara.co.in
Solara Active Pharma Sciences has been serving the global customers over two decades and having four USFDA audited sites and multiple times successfully audited by other global agencies like EDQM, MHRA, WHO (Geneva), PMDA ( Japan) and KDFA(Korea). Solara has large scale capacities to cater commercialization projects as well. We have an experienced pool of scientific team to help our global customers in discovery, development and commercialization projects in both non-GMP and GMP grade. With our world class infrastructure and experienced team, we will be able to fulfil all your chemical needs from Milligram to Metric tons quantity in custom synthesis, process R&D and cGMP manufacturing with best quality and within committed timelines
