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marketing@hengkangpharm.cn
Zhejiang Hengkang Pharma can supply this API with documents support.
gauravkumar4368@gmail.com
Dear Sir / Madam,
We can offer APIs along with the supporting documents.Kindly let us know yur email id so that we can send you the email and we can give you the best price.
Best Regards,
Gaurav Kumar
gauravkumar4368@gmail.com
Indo Pharm
INDIA
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
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
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
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
jason@greenbelt.cc
Dear Sir / Madam
This is Jason speaking.
Glad to hear that you are in the market for fenofibrate.
We have been in this product since 2006, hope to find a way to cooperate with you.
Await your immediate feedback.
Thanks
Best Wishes
Jason Bu
WhatsApp: +8613920852421
Email: jason@greenbelt.cc
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
sales@mishupharma.com
Dear Sir/ Madam,
We are a supplier based in India. Please let us know if we can work together?
You can visit our website www.mishupharma.in
Thanks & Regards
Mahima
himali.pawaskar@dksh.com
Hi ,please share this lead
contact@clearsynthlabs.com
Reply: Fenofibrate API
Clearsynth Labs is Manufacture/Wholesale Supplier of WHO cGMP, ISO, and GMP quality APIs, Intermediates, Excipients… with CoA, Chemical research… and services from India, UAE, Europe, Canada, US that meet customer and regulatory requirements (USDMF/CEP) compliance at a competitive price. Kindly contact us for your requirement.
Regards
17, Lotus Business Park
Andheri West
Mumbai - 400 053
Maharashtra State
Tel/WhatsApp: +91-8074411410
contact@clearsynthlabs.com
