26 May 2022

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Toluene as a Solvent needed in India [ENA13761]
A leading pharmaceutical company that focused in research, development and manufacturing of intermediates and APIs is looking for suppliers of Toluene as a Solvent for commercial purpose. The required quantity is 20 MT. The suppliers must support this enquiry with CoA.

Comments :

info@grefuel.com

Dear Sir/Madam,

Greetings from Grefuel Private Limited...!!

Hope you are doing well.

We are one of the leading manufacturer and supplier of Pharmaceutical bulk drug, Intermediates & Chemicals in India. It is available ready stock with us so, 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.

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)

15:14,  26 May 2022

arunodayalabs@gmail.com

We can supply 20MT Toluene

15:56,  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

22:38,  26 May 2022
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