16 Jan 2024

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Cannabidiol (10 g) API needed in Czech Republic [ENA18912]
A company that focuses on manufacturing and distribution of various finished formulations is looking for suppliers of Cannabidiol (10 g) API for development purposes. The suppliers must support this enquiry with CoA.

Comments :

Marketing.endo@pluviaglobal.com

Dear Friend
We believe that we can fulfill your requirements.
Please contact us on following details.
E-mail: Marketing.endo@pluviaglobal.com
Website: https://pluviaendo.com/

I’m waiting for your kind email.
Pluvia Consumer Health is a pharmaceutical company in Istanbul, Turkey. Our portfolio contains several specific #APIs & #Finished Dosage form medications in the field of Natural Opioid medications, #Cosmeceuticals & also #Nutraceutical Supplements.

11:32,  16 Jan 2024

sam.d@micoson.com

We will provide CBD quotation and document support, please send an email to sam.d@micoson.com, we will reply in time. Thank you.

20:41,  16 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

19:06,  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

11:33,  23 Jan 2024
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