Reply
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer Deoxycholic Acid API.Kindly let us know your email id so that we can send you the email and we can give you the best price.
Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA
crystalchemicalsfzllc@gmail.com
Crystal Chemicals FZ LLC is a supplier & Distributor of Active Pharmaceutical Ingredients (API’s) in Dubai, United Arab Emirates (UAE)
We can supply the following API, please contact
CRYSTAL CHEMICALS FZ-LLC
(Pharmaceuticals API's Distribution House in UAE)
Mobile & (Whatsapp) +971542360830
Email: crystalchemicalsfzllc@gmail.com
Website: www.crystalchemicals.ae
pharmchem1@ichemie.com
Greetings,
We are a company specializing in exporting a variety of high-quality APIs and intermediates.
We will not only provide high-quality and cost-effective APIs, but also provide high-quality after-sales service.
Looking forward to hearing from you so that we can communicate the details.
Yours sincerely,
Li Hao
Company: HANGZHOU ICH BIOFARM CO.,LTD.
Address: 1305, A Block, Dragon Times Center, 18 WanTang Road, Hangzhou, China
Whatsapp: +86-18771921569
Website: http://www.ichemie.com/
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life Sciences!!!
Hostrin offers the following services:
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.
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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.
3. Support for Impurity's, Reference standards and RLD's
4. Services for IPR & Regulatory compliance with all risk assessments.
5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.
6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.
7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.
8. Synthetic Resin technologies support.
9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.
10. Pharmacovigilance services.
Pls don't hesitate to send your inquiries. For your reference, please go through our website www.hostringlobal.com
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
info.upharma@gmail.com
Hello,
We can make a suitable offer for your above posted requirement. let me have your email ID to send you quotation.
For more check our website www.upharma.org
Team U Pharma
