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1. Linezolid 100 mg/5 ml suspension
2. Fluconazole 10 mg/ml suspension
3. Ciprofloxacin 250 mg/5 ml suspension
4. Itraconazole 10 mg/ml suspension
5. Nevirapine 50 mg/5 ml suspension
6. Oxybutynin hydrochloride 5 mg/5 ml syrup
7. Propranolol hydrochloride 20 mg tablets
durairaj.m@navitaslifesciences.com
We can help you with End-to-End regulatory services include - Submissions, Publishing, Dossier Management, CMC Management, Labeling and Artwork Management through a flexible, scalable and global delivery model. We have a good track record of effective submissions to global Health Authorities. In the past 6 years, we have done: 60,000+ eCTD, 20,000+ NeeS and 30,000+ paper submissions.
More details: www.navitaslifesciences.com
bd@ahslifesciences.com
Please share your email id to submit quote for EUCTD dossiers .
s.kapadiya@globi-corp.com
We can arrange dossiers and can provide technical services to ensure successful submission to MENA region
paavak.corporation@gmail.com
Kindly advise product specification, quantities, projected timelines and documentary/regulatory requirements
baschamconsultancy@yahoo.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
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
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
export@healthpharma.in
Dear Sir,
Good afternoon.
We can support you with all of your requirements. Kindly request you to send detailed email for ease of information.
Thank you.
