09 Apr 2022

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Tadalafil (300 kg) API needed in Italy [ENA13261]
An Italian CDMO that specializes in R&D and manufacturing of non-sterile medicinal products for human use is looking for suppliers of Tadalafil (300 kg) API for commercial purpose. The suppliers must support this enquiry with CEP.

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
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

11:39,  09 Apr 2022

info@eqpharma.com

We sell Tadalafil API along certification: CEP/COS; DMF, EDQM,FDA,Who gmp..
contact us for get our best quote: info@aeqpharma.com

16:18,  09 Apr 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting the following services.

1.We do support DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.

2. Impurity's & Reference standards support for API's

3. Services for IPR & Regulatory compliance

4. 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.

5. Custom synthesis and contract manufacturing services

6. Synthetic Resins technologies support.

7. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.

8. 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

22:22,  09 Apr 2022

Luisa.goglia@fischer-group.ch

Dear Sirs,

Kindly contact Fischer Chemicals aG

12:11,  11 Apr 2022

api@caren.se

Please send your full regulatory requirements to our email.
Our international team will be able to look into this for you.


Best Regards,
Ming Yuzhen (Marketing & Sales)

Tel: +8618411631209
Email: api@caren.se

01:12,  13 Apr 2022

himali.pawaskar@dksh.com

Hi , Please share this lead

09:44,  13 Apr 2022

jgq@yangzijiang.com

I am Justin from Yangtze River Pharmaceutical Group in China

APIs and generic Drugs (FDF) can be supplied by our company.

We can also CMO

If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com

20:18,  13 Apr 2022

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

13:43,  14 Apr 2022

Please contact.

14:33,  15 Apr 2022
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