05 Apr 2019

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CEP grade Levodropropizine API needed in Italy [ENA03850]
An Italian pharmaceutical group committed to research, development, manufacturing and commercialization of pharmaceutical products and active ingredients is looking for suppliers of CEP grade Levodropropizine API (150 kg). Suppliers must support the product with the below documents:
- EU GMP
- Written Confirmation
- Audit Report

Comments :

kaushal@newedgeoverseas.com

kindly share your requirement on below address
Thanks
kaushal

00:45,  06 Apr 2019

marketing@baschamlifesciences.com

Greetings from Bascham Life Sciences

We are pleased to inform you that we can support this requirement. Kindly share your contact details on our email to proceed further

Regards
Bascham Team, India

05:07,  06 Apr 2019

keysales@sina.com

Dear Sir,We want to promote the progress of levodropropizine,Please send the details to my email, and I will calculate and reply as soon as possible.
Thank you.

Mr. Key T

23:24,  07 Apr 2019

sales6@jiudianph.com

Dear Sir/ Madam,
Glad to know you looking for Levodropropizine, We China GMP manufacturer, supply CP/BP/EP standard levodropropizine.
Pls kindly contact with us for more informationt.
Luna
sales6@jiudianph.com

Hunan Jiudian Pharmaceutical Co., Ltd

11:55,  08 Apr 2019

aniketsheth123@gmail.com

USD180 PER kg CIF ITALY
CEP SUPPORT

17:33,  08 Apr 2019

hostrinlifesciences@gmail.com




Dear Friend,

Greetings from Hostrin Life sciences!!!

We have been supporting for the following services.

1.We do support DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/USA support in CTD, ACTD, eCTD and ANDA's formats with 5 modules including BA and BE studies /Clinical studies/trials for API's & Formulation's in Pharmaceutical, Ayurveda, Biotech, Biosimilar, vitamins , Peptides and recently Transdermal patches too.

2. Impurity's & Reference standards support for API's

3. Services for IPR & Regulatory compliance

4. 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.

5. Custom synthesis & Contract manufacturing services

6. Synthetic Resins technologies support

Pls don't hesitate to send your enquiry's. For your reference please go through our website www.hostringlobal.com

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

20:30,  19 May 2019
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