Reply
1. Entecavir (0.5 mg) Tablets. The required quantity is 975 units.
2. Tenofovir Disoproxil (245 mg) Tablets. The required quantity is 455 units.
sales@clearsynthlab.com
Reply:
1. Entecavir (0.5 mg) Tablets
2. Tenofovir Disoproxil (245 mg) Tablets
Clearsynth demonstrates the ability to consistently manufacture APIs, Intermediates, Chemical research, Finished Products… and services that meet customer and regulatory requirements. Kindly confirm your requirement by email so we can provide the Quotation...
Regards
Mr. V. Ambati
Plot No. 177, IDA
Mallapur
Hyderabad – 500076
Telangana State
Tel/WhatsApp: +91-9394436878
sales@clearsynthlab.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
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
namrata.sutphinrx@gmail.com
Sutphin Drugs Inc are licensed distributors of USFDA approved RLD’s,(Branded & Generic) Drug Products including controlled (Narcotic / Psychotropic) products sold in the United States
Kindly contact at info@sutphinrld.com or sutphinrx@gmail.com
namrata.sutphinrx@gmail.com
Sutphin Drugs Inc are licensed distributors of USFDA approved RLD’s,(Branded & Generic) Drug Products including controlled (Narcotic / Psychotropic) products sold in the United States
Kindly contact at info@sutphinrld.com or sutphinrx@gmail.com
dep5@techemi.com
Anhui Sinotech industrial co.,ltd one of the leading manufacturer, suppliers of API, Vet.-APIs,.We supply the APIS and documents. The goods is origin China .We can supply the COA and the goods package.. Please contact us : Xu ping
Anhui Sinotech Industrial Co.,Ltd
Tel: 86-551-65692531
Whatsapp/Mob: 0086-13866721542
Email: dep5@techemi.com
Web: http://www.techemi.com
sales@winergy.in
We make everything on order at our FDA approved plant. Goods are manufactured in India. COA & all necessary documentation taken care of till delivery to your port. Reach out over email/whatsapp to discuss further, take quote & close order!
Whatsapp - +91 9718972797
Email - sales@winergy.in
