22 Jun 2022

Reply

Compacted & Micronized Azithromycin API needed in Bangladesh [ENA14054]
A company that deals in trading and distribution of various pharmaceutical products is looking for suppliers of Compacted Azithromycin (500 kg) & Micronized Azithromycin (300 kg) API for commercial purpose. The suppliers must support this enquiry with CoA.

Comments :

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

15:15,  22 Jun 2022

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.

16:25,  22 Jun 2022

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

06:17,  23 Jun 2022

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

18:29,  25 Jun 2022
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty