14 Jul 2022

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Suramin API needed in the United States [ENA14329]
A company that deals in various pharmaceutical products is looking for suppliers of Suramin API for commercial purpose. The suppliers must support this enquiry with CoA.

Comments :

SALVAVIDAS PHARMACEUTICAL PVT.LTD

We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.

We are dealing in Active Pharmaceutical Ingredients (API’s), Veterinary APIs, Intermediates, Excipients & Chemicals… We deal with Branded Drugs along with all Related Documents and Certificates.

We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.

We are looking forward to your early reply to establishing a business relationship with your company.

We are always there to serve you with our best services

All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.

Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com

10:21,  14 Jul 2022

bdevomaar@gmail.com

Dear
Please send the inquiry on below email.
We can support your requierment for the API.
bdevomaar@gmail.com

11:06,  14 Jul 2022

info@aeqpharma.com

we sell Suramin API along full support Docs

13:37,  14 Jul 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting 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 and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.

3. Impurity's & Reference standards support for API's

4. Services for IPR & Regulatory compliance

5. Services for QMS & supporting of QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars companies who are willing to enter into the Regulatory market which is mandatory to show for FDA.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PD 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

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

21:54,  14 Jul 2022

himali.pawaskar@dksh.com

Hi, Share this lead

09:55,  20 Jul 2022
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