23 Nov 2022

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Looking for a FDA/ EU GMP certified CDMO for Injectables [ENA15629]
A specialty biopharma company that deals in innovation, reinvention and optimization of existing medications is looking for a FDA/ EU GMP certified Sterile CDMO for Freeze Drying on organic solvents based Injectable Formulation (TBA 50 to 60% content). The projected manufacturing volume is 250,000 - 500,000 vials/ annum. The required packaging is clear and amber glass vial of 10 ml. The current project is in Phase 3. The country of distribution is US and Worldwide. The project will launch in 2025.

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

18:08,  23 Nov 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

For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

00:52,  24 Nov 2022

dep5@techemi.com

Anhui Sinotech industrial co.,ltd one of the leading manufacturer, suppliers of API, Vet.-APIs,.We supply the APIS and documents. The goods is origin China .We can supply the COA and the goods package.. Please contact us : Xu ping

Anhui Sinotech Industrial Co.,Ltd
Tel: 86-551-65692531
Whatsapp/Mob: 0086-13866721542
Email: dep5@techemi.com
Web: http://www.techemi.com

06:47,  24 Nov 2022

oscar_j_l@hotmail.com

I´m cooperating with Scandinavian company specialized in production of injectable products.

Would be glad to discuss possible business cooperation.

22:00,  07 Dec 2022

ajay.p@itaanpharma.com

Our site with Lyo will be inspection ready in a few months. Contact us for further details: https://itaanpharma.com/

10:17,  07 Jan 2023

tutuwc@126.com

We have both FDA/EU certified production workshop based in China for your requirements with cost competative, pls do not hesitate to contact.

08:41,  31 Mar 2023

assem_ezzeldin@globalnapi.com

EU GMP certified, Global Pharmaceutical Industries, Egypt.
One of the the leading manufacturer and exporter of injections to Latin American countries, Africa, Gulf & Asian, Azerbaijan, Belarus, Uzbekistan Russia, and Tajikistan.
for More info, please contact me by:
email: assem_ezzeldin@globalnapi.com
WhatsApp: +201023977115

15:11,  30 Oct 2023
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