Reply
sales1@jnchsd.com
Dear Sir/Madam:
Greetings of the day. We are The Manuafacturer’s of API and Intermediates.
We, Shandong Chenghui Shuangda Pharmaceutical Co.,Ltd, are cGMP plant who manufacrtures the APIs and intermediates. Some of our major products are mentioned below:
Vonoprazan Fumarate
LeterMovir
Dapagliflozin
Crisaborole
Sugammadex
Ropivacaine HCI
Tetracaine HCI
Tetracaine
Prilocaine
Lidocaine
Ozagrel Sodium
Celecoxib
Pramoxine HCI
Meldonium
We could supply above APIs and their main intermediates. If you are intrested in any of them,please feel free to contact me by sales1@jnchsd.com Tel:86-531-58897062,
Fiona
alicechan@huarizy.com
HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.
1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80
email address: alicechan@huarizy.com
phone number: +86 18820220687
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
himali.pawaskar@dksh.com
Hi, Please share this lead
export@paradisehealthcare.in
PARADISE HEALTHCARE
we have our own GMP approved manufacturing plant in Vodadara where we manufacture - Montelukast Sodium USP, Memantine HCL , Dapagliflozin and Lornoxicam.
Please connect for COA and QUOTATION.
Mob - +919892486840
