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1. 7-Hydroxy-2-oxo-1,2,3,4-tetrahydroquinoline (CAS 22246-18-0) Intermediate
2. 2-Phenylethylamine (CAS 64-04-0) Intermediate
3. Ethyl 2-amino-4,5-bis(2-methoxyethoxy)benzoate hydrochloride (CAS 183322-17-0) Intermediate
bioquantumpharma@gmail.com
Greetings from BIO QUANTUM PHARMA
We are ready to supply as per your requirement with lead time and against proforma invoice
Thanks
Bio Quantum Pharma
77949 86845
sales6@iffect.com.cn
Greetings from Iffect Chemphar Co., Ltd!
IFFECT CHEMPHAR CO., LTD. is one of the biggest R&D and manufacturer base specialized in new and high valued added APIs in China, we are both manufacturer and exporter for Pharmaceuticals & Veterinary API and its main intermediates. And now we are on the way to apply for COS and FDA approval for some of our products. Meanwhile we are also willing to register our products in your market if it's requested.
We have intermediates
(CAS 22246-18-0) 98% assay
(CAS 64-04-0) 98% assay
(CAS 183322-17-0) 98% assay
More information needed, please feel free to contact.
NouryonChemltd@gmail.com
We can handle to supply your required products and other various APIs from USA.
Email: NouryonChemltd@gmail.com, NouryonChemltd@outlook.com
Skype ID: NouryonChemltd
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
