20 Jan 2024

Reply

Testosterone Undecanoate (10 kg) API needed in Spain [ENA18933]
A company that focuses on manufacturing and development of cosmeceutical, nutraceuticals, class III intradermal administration medical devices, topical drugs as well as energy based medical aesthetic devices is looking for suppliers of Testosterone Undecanoate (10 kg) API for development purposes and later commercial. The suppliers must support this enquiry with EU-DMF & CoA.

Comments :

haoran.tse@gmail.com

we can supply, manufactured in China.

16:47,  20 Jan 2024

bdevomaar@gmail.com

Dear Sir,
Please send the requierment on below email.
We can provide the API along with USDMF.
bdevomaar@gmail.com
Kind regards

14:54,  21 Jan 2024

service5@dragonpharm.com.cn

Hangzhou Dragonpharm can supply this API.

08:28,  22 Jan 2024

export3@zealmp.com

Dear Sir, Greetings from Zeal Medipharma Export India.
We are Government of India Recognized Star Export House based in Mumbai India, currently exporting wide range of APIs to more than 40 countries.
Please send your valuable purchase inquiry on export3@zealmp.com. We will be glad to submit our best offer.

Best Regards,
Ashvi Panchal
Business Development
Zeal Medipharma
(EXPORT) PRIVATE LIMITED
Mumbai, India
Tel: +91-22-25836688
Mobile : +91 9867166055
E-mail : export3@zealmp.com

15:25,  22 Jan 2024

Cristonelifecare@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.

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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance with all risk assessments.

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. 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
www.hostringlobal.com

18:58,  22 Jan 2024

export3@zealmp.com

Dear Sir, Greetings from Zeal Medipharma Export India.
We are Government of India Recognized Star Export House based in Mumbai India, currently exporting wide range of APIs to more than 40 countries.
Please send your valuable purchase inquiry on export3@zealmp.com. We will be glad to submit our best offer.

Best Regards,
Ashvi Panchal
Business Development
Zeal Medipharma
(EXPORT) PRIVATE LIMITED
Mumbai, India
Tel: +91-22-25836688
Mobile : +91 9867166055
E-mail : export3@zealmp.com

09:40,  23 Jan 2024

export3@zealmp.com

Dear Sir, Greetings from Zeal Medipharma Export India.
We are Government of India Recognized Star Export House based in Mumbai India, currently exporting wide range of APIs to more than 40 countries.
Please send your valuable purchase inquiry on export3@zealmp.com. We will be glad to submit our best offer.

Best Regards,
Ashvi Panchal
Business Development
Zeal Medipharma
(EXPORT) PRIVATE LIMITED
Mumbai, India
Tel: +91-22-25836688
Mobile : +91 9867166055
E-mail : export3@zealmp.com

09:41,  23 Jan 2024

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

12:52,  23 Jan 2024

Cristonelifecare@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers the following services:

1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA formats. DMF support for API's as well.

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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance with all risk assessments.

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. 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
www.hostringlobal.com

17:16,  23 Jan 2024

sales@mishupharma.com

Dear Sir/ Madam,

We are a supplier based in India. Please do let us know if we can work together?

Thanks & Regards
Mahima

09:23,  26 Jan 2024
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