Reply
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer APIs along with the supporting documents.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
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
www.hostringlobal.com
info@shreechemicalsimpex.com
Hello,
We, "SHREE CHEMICALS IMPEX " are contract manufacturer, supplier and exporter of active pharmaceutical ingredient, pharmaceutical intermediate and agrochemicals.
We can fulfill your requirements.
Please contact on following details.
E-mail : info@shreechemicalsimpex.com
Mo-no : (+91) 8200048670
snamarketing1@gmail.com
hello,
WE SNA health care, a WHO GMP , ISO certified factory from India. We manufacture API and intermediates and supply globally. Pls email your inquiry to - snamarketing1 @ gmail . com
joseph.travasso@tenatra.com
is interested
Krishna.Prasad@tagoorlabs.com
We are most competitive in the world for Loratadine and completely backward integrated with full documentation.
Krishna.Prasad@tagoorlabs.com
We are most competitive in the world for Loratadine and completely backward integrated with full documentation.
info.upharma@gmail.com
Hello,
We can supply your said API. Let me have your email ID to share the quotation with COA & other documents.
For more visit our page https://www.upharma.org/
Team U Pharma
marketing@vasudhapharma.com
Yes we can supply Loratadine API with CEP and from USFDA approved facility. Please send a mail to the above id
sales@activepharma.co.uk
ACTIVE PHARMA SUPPLIES can support you with supply of this API. Please contact our sales team at sales@activepharma.co.uk
