A fast-growing, innovative consumer healthcare company in Europe is looking for contract manufacturers to produce tablets for a cytotoxic new drug.
Hi Our facility EU GMP approved for cytotoxic products. please share further details.
09:28, 17 Feb 2019
19:31, 18 Feb 2019
We would be glad to work on this project. I would be glad to take this forward if you could drop me an email.
21:06, 21 Feb 2019
15:43, 23 Feb 2019
Kindly advise product specification, quantities and projected timelines
23:54, 26 Feb 2019
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 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
CEO & Managing Director
Hostrin Life sciences
WhatsApp: +91 9949930343
14:33, 06 Mar 2019
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