19 Jun 2023

Reply

Methenamine Hippurate (MOQ) API needed in Bangladesh [ENA17349]
An indenting company that deals in the distribution of various pharmaceutical products is looking for suppliers of Methenamine Hippurate (MOQ) API for commercial purposes. The suppliers must support this enquiry with CoA.

Comments :

gauravkumar4368@gmail.com

Dear Sir / Madam,

We can offer APIs along with the supporting documents.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
gauarvkumar4368@gmail.com
Indo Pharm
INDIA

16:35,  19 Jun 2023

arslan@risenchemicals.com

We can supply the same from our WHO/GMP USFDA approved sources,please revert via email or WhatsApp for more details.

Regards
Ali Arslan
WhatsApp: 00923214949909
Email: arslan@risenchemicals.com

14:36,  20 Jun 2023

info@shreechemicalsimpex.com

Hello,
We, "SHREE CHEMICALS IMPEX " are contract manufacturer, supplier and exporter of active pharmaceutical ingredient, pharmaceutical intermediate and agrochemicals.
We can fulfill your requirements.
Please contact on following details.
E-mail : info@shreechemicalsimpex.com
Mo-no : (+91) 8200048670

21:11,  20 Jun 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. DMF's for API's, 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 software, addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance

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.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

9. 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

01:36,  21 Jun 2023

himali.pawaskar@dksh.com

Hi,Please share this lead

09:02,  21 Jun 2023

pharmatechhng@gmail.com

Sir,

We Pharmatechh NexGen, Mumbai are into API business of India origin products.

We can cater to your API requirements with supporting documents on regular basis directly from our associate manufacturers.

Please let us know your exact requirements along with port of destination. We will quote best possible lowest price.

Looking forward to your reply.

With regards,
Milind Sawant
Pharmatechh NexGen
Mumbai. India
M: +91/9322120615
pharmatechhng@gmail.com

15:21,  28 Jun 2023
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