A fast-growing, innovative consumer healthcare company in Europe is looking for contract manufacturers to produce tablets for a cytotoxic new drug.

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bd@ahslifesciences.com

Hi Our facility EU GMP approved for cytotoxic products. please share further details.

09:28,  17 Feb 2019
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comercial@latac.es

please conntact us

19:31,  18 Feb 2019
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geetha@qualitepharma.com

Hi,
We would be glad to work on this project. I would be glad to take this forward if you could drop me an email.

21:06,  21 Feb 2019
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arrowindustries15@gmail.com

pl.contact to us

15:43,  23 Feb 2019
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paavak.corporation@gmail.com

Kindly advise product specification, quantities and projected timelines

23:54,  26 Feb 2019
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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

14:33,  06 Mar 2019
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