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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)
chowdary@carbontree.in
Dear Sir,
We can supply Malathion USP from our WHOGMP facility and we have USFDA audit on 6th June2022.
www.basislaboratories.co.in
bd@basislaboratories.co.in
info@spentose.com
Hi,
We are the largest manufacturers of pure Melatonin pharmaceutical grade API.
Our facility is USFDA inspected and approved, WHO-GMP certified and compliant with major regulatory bodies worldwide.
We have our USDMF filed as well with the USFDA. We also have our ASMF filed in multiple EU countries, UKMHRA and TGA.
We are selling our Melatonin API Globally.
We can offer both USP and EP.
Please reach out to us for more information at info@spentose.com
Regards,
Lynette
luisa.goglia@fischer-group.ch
Please contact Fischer Chemicals in Swizerland.
Thank you.
narendra@anaxlab.com
Dear, We Anax Laboratories are producers of Melatonin USP and Melatonin BP grade.
request you to kindly contact for your valuable requirement
Anax Laboratories
rakesh@anaxlab.com
info@anaxlab.com
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
