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sales@clearsynthlab.com
Reply: D-Glucosamine HCl (CAS 66-84-2) Intermediate
Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research… and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation, COA...
Regards
Mr. V. Ambati
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
www.clearsynthlab.com
Tel/WhatsApp: +91-9394436878
sales@clearsynthlab.com
chowdary@carbontree.in
Dear Sir,
We can supply D-Glucosamine hcl from our GMP facility
susie@further-pharm.com
Dear sir/madam
Good day. Please allow me introduce our company. WuXi Further Pharmaceutical is a company that researches, produces and sells APIs, pharmaceutical intermediates and healthcare products. So we can meet your demand. In addition, we can offer you COA and ISO. Please be assure to purchase it. Whatsapp:+86 18036885286
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) 8000239721
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
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
navee@chemyzolab.com
Dear sir/mam ,we are into API,Intermediates,speciality chemicals,Custom synthesis manufatcuringPlease write your requirements to navee@chemyzolab.com
Regards,
NAVANEETHAKRISHNAN.G
Founder and Director of CHEMYZOLAB(P)Ltd
Dreamer, Imaginator, Creator, Entrepreneur
Bangalore-INDIA
BusinessDevelopment
WhatsApp : +91 9558347707
Cell Number :+91 9558347707
navee@chemyzolab.com
www.chemyzolab.com
