03 Jun 2022

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USP/ NF Grade Sodium Bisulfite (10 kg) Excipient needed in Slovenia [ENA13842]
A global pharmaceutical company that focuses in research, development and manufacturing of generic pharmaceuticals and biosimilars is looking for suppliers of USP/ NF Grade Sodium Bisulfite (10 kg) Excipient for development purpose. The suppliers must support this enquiry with GMP.

Comments :

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

10:47,  03 Jun 2022

Respected sir/ ma'am,
I am Rohan from Salvavidas Pharmaceutical Pvt. Ltd. India & hope you are fine!
We are involved in manufacturing, supplying, and exporting all types Of APIs, intermediate and Excipients in more than 30 Countries and hold a Prominent Exporter.
If you have any requirements, doubts or queries then feel free to contact us.
We are looking forward to your early reply to establishing a business relationship with your company..
For more Faster and Efficient Communication, Please connect with us via9313237877

17:15,  03 Jun 2022

marketing.neion@gmail.com

Hello Sender,
Please share your contact details to discuss further on this inquiry.

14:25,  04 Jun 2022

SALVAVIDAS PHARMACEUTICAL PVT.LTD

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

We deal with Finish Products, Surgical items. We also Deal with Branded Drugs along with all Related Documents and Certificates.

We are also dealing in Active Pharmaceutical Ingredients (API’s), Intermediates, Excipients & Chemicals…
We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.  
If you have any requirements, doubts or queries then feel free to contact us.

We are always there to serve you with our best services


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

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

18:07,  06 Jun 2022

himali.pawaskar@dksh.com

Hi, Please share this lead

11:40,  10 Jun 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

17:57,  25 Jun 2022
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