Reply
The deadline is 20-Jan-2021.
pharmahouse@ymail.com
We are providing below services required people contact privately.
Dossiers (CTD, e-CTD, ANDA and ANVISA)
DMFs(CTD, e-CTD)(Open &Closed part)
Technology transfers(API'S &Formulations),
Pharmacovigilance(PV),
Intellectual properties(IP)
Product Development for API'S &Formulations.
&other Regulatory services.
Pharma House,
pharmahouse@ymail.com ,
Hyderabad, India
Whats App&Voice:+91 7799500435
enquiry@artempharmas.com
Greetings from ARTEM Pharma (www.artempharmas.com).
Please get in touch with us to proceed with your requirements we are in position to support.
vishvesh.shaishav@gmail.com
We are a one of the leading Indian manufacturer, supplier, importer, dealer, distributor, trader, exporter that is used in pharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, additives, contract manufacturing, chemical compound for pharmaceutical and chemicals process industry available at best price
We are exporting several of our products to Latin American countries, Gulf & Asian countries and also a few products to Australia, UK & USA.
Regulatory documents service etc.
Vishvesh.shaishav@gmail.com
jgq@yangzijiang.com
jgq@yangzijiang.com
I am Justin from Yangtze River Pharmaceutical Group in China
APIs and FDF can be manufactured by our company.
We can also CMO
If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com
hostrinlifesciences@gmail.com
Dear Friend,
Greetings from Hostrin Life sciences!!!
We have been supporting the following services.
1.We do support DMF for API, Tech transfer support and Registration of Dossiers in ROW/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 & Formulations 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
