18 Aug 2022

Reply

Various Excipients needed in Mexico [ENA14720]
A pharmaceutical company that focuses on the development, manufacturing, marketing and distribution of generic drugs, primarily prescription, OTC, medical devices, and cosmetics is looking for suppliers of Various Excipients for development purpose. The required quantity is 1 kg/annum for each. The suppliers must support this enquiry with DMF, GMP & CoA.
1. Polyethylene Glycol 400 Excipient
2. Propylene Glycol Excipient

Comments :

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
Whatsapp +91 9033215377
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVE

08:32,  18 Aug 2022

tianranbiotechz@gmail.com

Our company is located in Uganda, Africa. The factory directly supplies medical bovine skin gelatin, which is suitable for capsules, soft gel, etc. welcome to negotiate and cooperate.
We are a manufacturer with many international certifications, including FDA, ISO 22000, FSSC22000, Halal, GMP, BRC and other certifications.
Whatsapp:+256 705290608

E-mail: tianranbiotechz@gmail.com

PLOT 5-7 NYANZA CLOSE JINJA

P.O.BOX 33695 KAMPALA UGANDA

13:13,  18 Aug 2022

tianranbiotechz@gmail.com

Our company is located in Uganda, Africa. The factory directly supplies medical bovine skin gelatin, which is suitable for capsules, soft gel, etc. welcome to negotiate and cooperate.
We are a manufacturer with many international certifications, including FDA, ISO 22000, FSSC22000, Halal, GMP, BRC and other certifications.
Whatsapp:+256 705290608

E-mail: tianranbiotechz@gmail.com

PLOT 5-7 NYANZA CLOSE JINJA

P.O.BOX 33695 KAMPALA UGANDA

13:13,  18 Aug 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 manufactures 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,
Whatsapp/Wechat/Skype: +86 18605387751
Fiona

13:05,  19 Aug 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

19:25,  01 Sep 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