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info@aeqpharma.com
Dear Sir,
we have Chondroitin Sulfate API along full support docs.DMF;GMP,EDQM..etc
contact us for get our best quote
info@aeqpharma.com
luisa.goglia@fischer-group.ch
PLEASE CONTACT Fischer Chemicals AG
Thank you
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
SALVAVIDAS PHARMACEUTICAL PVT.LTD
We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.
We are dealing in Active Pharmaceutical Ingredients (API’s), Veterinary APIs, Intermediates, Excipients & Chemicals… We deal with Branded Drugs along with all Related Documents and Certificates.
We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.
We are always there to serve you with our best services
All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.
Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com
sales@gmfclabs.com
Dear Sir,
Please send us inquiry on below email.
We can support your requirement for the API 's with all documents.
sales@gmfclabs.com
regards
GMFC LABS PVT LTD
Hi,
We are professional in sourcing API’s to many countries. We can source a good company for required API with all documents like Mfg license, GMP and DMF. Do let us know if we can have a cooperation for the same.
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
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