Reply
info@biopharmacentrum.com
Hi,
We can support with very economical price and quality and regulatory complied source for this product. Please send your formal inquiry for any kind of API, Intermediate, Excipients and other raw materials at :-
"info@biopharmacentrum.com"
Mob: +91 89514 33372
b.teymuri@pharmanova.ae
Dear Sir/ Madam,
Greetings.
I would like to inform you that we can support you with your inquiry. Please send me an email to discuss this matter further.
Best regards,
Bahar Teymuri
b.teymuri@pharmanova.ae
+971 52316 0905
b.teymuri@pharmanova.ae
Dear Sir/ Madam,
Greetings.
I would like to inform you that we can support you with your inquiry. Please send me an email to discuss this matter further.
Best regards,
Bahar Teymuri
b.teymuri@pharmanova.ae
+971 52316 0905
hostrinlifesciences@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
bd@indivarsciences.com
Hello Sir/Madam,
Indivar Sciences is a trusted supplier of high-quality APIs and Intermediates serving the pharmaceutical and compounding industries globally we are committed to providing top-tier products with full documentation to ensure quality and compliance. We would welcome the opportunity to discuss how we can support your needs and collaborate on future projects.
Best regards,
Keerthi.
bd@indivarsciences.com
91 9848049199
Indivar Sciences private limited
www.indivarsciences.com
info@chemcon.com
Dear Sir or Madam,
ChemCon is a supplier of high quality APIs produced in Germany. We are able to deliver APIs with all the neccessary analytics for your use case and the appropriate documentation. Histaminedihydrochloride is one of our commercially avaiable GMP products. We do have a valid DMF for this API in particular.
If you need high quality and regulatory support ChemCon would be the way to go.
Regards your ChemCon team.
