Reply
paavak.corporation@gmail.com
Please advise quantities and timelines
shahab@keyperpharma.com
we can supply, please share more details at shahab@keyperpharma.com
baschamconsultancy@yahoo.com
Greetings from Bascham Life Sciences
We are pleased to inform you that we can support this requirement. Kindly share your contact details on our email to proceed further
Regards
Bascham Team
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 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
comercial@latac.es
you can contact us
comercial@latac.es
