21 Jul 2023

Reply

Valproic Acid (500 mg) Enteric Release Tablets needed in Chile [ENA17626]
A global leading pharmaceutical company that focuses on research, development and manufacturing of finished formulations for pain management and related diseases is looking for suppliers of Valproic Acid (500 mg) Enteric Release Tablets for commercial purposes. The suppliers must support this enquiry with dossier.

Comments :

drniral@medwiseoverseas.com

Dear Sir/Madam
Greetings of the day!!Namaste!!
We can surely supply the same with needed dossier.
Please contact me on WhatsApp on + 91 9909986882 & email id : drniral@medwiseoverseas.com

Thanks & Regards
Dr Niral Patel
www.medwiseoverseas.com

23:33,  22 Jul 2023

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

01:33,  25 Jul 2023

Good day,

We can offer along with ready dossier, do let us know the volumes.

16:07,  25 Jul 2023

Good day,

We can offer along with ready dossier, do let us know the volumes.

16:07,  25 Jul 2023

inquiry@remedypharma.co.in

We can support the inquiry from our Eu-GMP factory along with the dossier.

12:16,  28 Aug 2023
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