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1. Drotaverine HCl (20 mg/ ml) Solution for Injections. The required quantity is 1,800 units.
2. Tranexamic Acid (100 mg/ ml in 5 ml) Solution for Injections. The required quantity is 2,400 units.
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arkribio@gmail.com
Dear Sir/Madam
We ArKri Biopharm is a India based distributor and exporter of pharmaceuticals, dietary supplements and medical devices from India.
Please let us know your documentation requirements for proposed products (i.e Full dossier or Partial dossier or Limited documents like CoA, GMP certificates etc.,)
Your quick response is highly appreciated.
Thank you so much.
Best Regards
Dr. Bela
ArKri Biopharma
India
arkribio@gmail.com
Whats App: +917861047633
arkribio@gmail.com
Dear Sir/Madam
We ArKri Biopharm is a India based distributor and exporter of pharmaceuticals, dietary supplements and medical devices from India.
Please let us know your documentation requirements for proposed products (i.e Full dossier or Partial dossier or Limited documents like CoA, GMP certificates etc.,)
Your quick response is highly appreciated.
Thank you so much.
Best Regards
Dr. Bela
ArKri Biopharma
India
arkribio@gmail.com
Whats App: +917861047633
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life Sciences!!!
Hostrin offers the following services:
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.
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
