25 May 2022

Reply

Bismuth Subnitrate API needed in Ireland [ENA13751]
A company that focused in manufacturing of various pharmaceutical products for veterinary use is looking for suppliers of Bismuth Subnitrate API for commercial purpose. The suppliers must support this enquiry with CEP, DMF and CoA.

Comments :

aniketsheth123@gmail.com

Hey Sir/Madam,

Bismuth Subnitrate , how much qty you require in first order?

CEP or DMF require mandatory?

Are you end user?

Delivery require in ireland?

We have INDIAN or CHINESE sources, all are workable for you source?

What is your target price?

Revert us by email , so we quote you!

Thanks & regards,

Aniket

CEO

Anshvansh trading
WhatsappMobile :+91-9558577600
Mobile :+91-8160513359
Email : Aniketsheth123@gmail.com
Shethaniket644@yahoo.com

19:57,  25 May 2022

aniketsheth123@gmail.com

Hey Sir/Madam,

Bismuth Subnitrate , how much qty you require in first order?

CEP or DMF require mandatory?

Are you end user?

Delivery require in ireland?

We have INDIAN or CHINESE sources, all are workable for you source?

What is your target price?

Revert us by email , so we quote you!

Thanks & regards,

Aniket

CEO

Anshvansh trading
WhatsappMobile :+91-9558577600
Mobile :+91-8160513359
Email : Aniketsheth123@gmail.com
Shethaniket644@yahoo.com

19:57,  25 May 2022

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

22:04,  25 May 2022

info@grefuel.com

Dear Sir/Madam,

Greetings from Grefuel Private Limited...!!

Hope you are doing well.

We are one of the leading manufacturer, supplier and exporter of Pharmaceutical bulk drug and its Intermediates & Chemicals in India. If you have any requirement for the same, please send us your valuable email on info@grefuel.com We will be pleased to offer you our competitive prices with prompt delivery.

Our manufacturing plant as per GMP guidelines which itself shows our commitment to strict quality standards set by National & International Regulatory compliances.

Looking forward to a new business relationship with you.

Thanks & Regards
Pratik Patel
Grefuel Private Limited
F-14, Lakeview Plaza, Opp. GIDC Lake,
GIDC, Ankleshwar, Bharuch, Gujarat,
India - 393 002
Mob. +91 91731 91981 (WhatsApp)

15:36,  26 May 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

22:43,  26 May 2022
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