08 Oct 2024

Reply

Ephedrine Anhydrous API needed in Kenya [ENA20785]
A company that focuses on the manufacturing of various pharmaceutical, OTC and FMCG finished formulations is looking for suppliers of Ephedrine Anhydrous API for commercial purposes. The suppliers must support this enquiry with GMP, ODMF & CoA.

Comments :

avinash@dvsrlifesciences.com

We can Supply Ephedrine Hcl we can get in touch and discuss this further Please contact E-mail:avinash@dvsrlifesciences.com
Ph No: +91 9121391234.

16:39,  08 Oct 2024

sales@elevenclockhealthcare.com

Dear sir

We will provide you as per your requirements of API.

Can you share me your contact.

22:08,  08 Oct 2024

kawtarettayri@zintellec.com

Dear Sir/Madam,
ZIntellec Chemical is a reliable Chinese supplier of high-quality APIs and pharmaceutical intermediates, catering to the global pharmaceutical and compounding industries. We are dedicated to delivering premium products, backed by full documentation to ensure both quality and compliance.
We would be delighted to explore how we can meet your business needs and collaborate on future projects.

Best regards,
Kawtar
http://www.zzhxchem.com
ZIntellec Chemical & Tech. Co., Ltd

06:49,  09 Oct 2024

hostrinlifesciences@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

15:01,  12 Oct 2024

gautam@dmpharma.in

Please send us your Requirement via, We can offer with DMF if required.
gautam@dmphamra.in

Regards
DM Pharma / APC

12:13,  17 Oct 2024
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