A company is looking for CMOs to manufacture formulations for controlled substances in pellets. Manufacturers must comply with the regulatory license to handle the DEA (Schedule 2). Volume forecast is 12-20 ton per year.
22:24, 20 May 2019
Greetings from GBS Organics.
We are pleased to inform you that we can support this requirement. Kindly share your contact details on our email to proceed further
Kindly send us above information soonest possible.
11:35, 21 May 2019
A EU company from our network can handle products according DEA schedule. Company is interested in pellets production.
Please contact us. Thanks in advance.
13:06, 23 May 2019
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
CEO & Managing Director
Hostrin Life sciences
WhatsApp: +91 9949930343
15:31, 04 Jun 2019
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