Reply
vijay@jackrabbit.in
We can offer you the same
please contact us on email
hostrinlifesciences@gmail.com
Hostrin Life Sciences
*One Stop For Pharmaceutical and Biosimilar Regulatory Solutions.
Hostrin offers the following services:
1.Out-licensing Dossiers
2.Dossiers in CTD/ACTD/eCTD formats
3.CDMO (Contract Research & Development)
4.Tech transfer support and Registration of Dossiers in all markets.
5.eCTD publishing with potential softwares and addressing post submission queries from all regulatory authorities.
6.QBD & QMS_Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP Assessment Audits.
7.BE studies and clinical studies from US-FDA, EU-GMP, UK-MHRA, TGA-Australia/GCC/ANVISA approved CRO's/BE Study Centers.
8.Synthetic Resin technologies support.
9.Cleaning validation/ toxicology study reports (PDE/ADE I OEL) values for API's & FDF's
10.Pharmacovigilance
Pls don't hesitate to send your inquiries. 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
www.hostringlobal.com
himali.pawaskar@dksh.com
Hi ,please share this lead
