Reply
foramjjani@gmail.com
Hello,
I am Foram from India. I provide assistance for regulatory & QA documents like DMF, dossier, PV, AMV etc. Whtsapp: +919819435009
Vishal@siddhint.com
We would like to introduce our company for you as one of the well established Manufacturers, Contract Manufacturers, Exporters and Importers in the field of Pharmaceutical Raw Materials/API's, Veterinary, Nutraceutical/Herbal Extracts, Chemicals. We are in this field for more than 25 years and supplying to more than 35 countries to 100's of our customers with full Documentation support as required.
We are glad to offer our complete range of products on our web www.siddhint.com
Vishal Goenka
ross@integral-biopharma.co.uk
Good day
Please touch base with us so we can assist you further.
Regards
Ross
info@biopharmacentrum.com
Hi,
We can supply this product, having cost effective and quality & regulatory complied. Please send your inquiry for any products at "info@biopharmacentrum.com" or Whatspp +91 89514 33372
Thanks.
Cristonelifecare@gmail.com
Dear Friends,
Greetings from Hostrin Life Sciences!!!
Hostrin offers the following services:
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biosimilars, Nutraceutical, Biotech and in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.
CDMO (Contract research, development and manufacturing organisation) activity and growing rapidly. Offering drug product development services from Active pharmaceutical ingredient to Formulation development and manufacturing for all the markets with relevant regulatory requirements.
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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance with all risk assessments.
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.
7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.
8. Synthetic Resin technologies support.
9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.
10. 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
www.hostringlobal.com
