24 Aug 2023

Reply

USP Grade Trichlorfon API needed in Bangladesh [ENA17883]
A company that deals in various pharmaceutical products is looking for suppliers of USP Grade Trichlorfon API for commercial purposes. The suppliers must support this enquiry with CoA.

Comments :

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer Trichlorfon API.Kindly let us know your email id so that we can send you the email and we can give you the best price.

Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA

17:56,  24 Aug 2023

marketing@orionpakistan.com

Dear Sir/Madam

We can supply you this item from good source at very good price , please contact us via email

marketing@orionpakistan.com
Abdul Saboor LOdhi
Contact : +92-339-4002426
www.orionpakistan.com

21:59,  24 Aug 2023

abul.hasan@acigodrej.com

I have required Trichlorfon usp powder API quality. First time required 25 kg or 1 dram to trial purpose and next time the product will be required more. If you want to help me then you can do.

23:04,  24 Aug 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
www.hostringlobal.com

19:36,  27 Aug 2023
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