Reply
sales@neochempharma.com
We can supply Eslicarbazepine please contact us for your requirement of API & EXICIPIENTS.
Dr Madhavi patel
Email : sales@neochempharma.com
Mobile : +91 8320528643
foramjjani@gmail.com
Hello,
Greetings for the day!
My name is Foram Jani from Mumbai, India, Asia.
Regulatory service: I provide end to end product registration support like compiling a dossier in CTD, ACTD format based on country-specific requirements as well as query resolution. I can also prepare DMF, PV, COA, FPS, RMS, AMV and all pharma technical documents.
--
Warm Regards,
Ms. Foram Jani
Regulatory affairs specialist
Contact: +919819435009
Email: foramjjani@gmail.com
foramjjani@gmail.com
Hello,
Greetings for the day!
My name is Foram Jani from Mumbai, India, Asia.
Regulatory service: I provide end to end product registration support like compiling a dossier in CTD, ACTD format based on country-specific requirements as well as query resolution. I can also prepare DMF, PV, COA, FPS, RMS, AMV and all pharma technical documents.
--
Warm Regards,
Ms. Foram Jani
Regulatory affairs specialist
Contact: +919819435009
Email: foramjjani@gmail.com
pratik.tantia@alkem.com
We can supply Eslicarbazepine along with USDMF. Please contact us.
hostrinlifesciences@gmail.com
Hostrin Life Sciences
*One Stop For Pharmaceutical and Biosimilar Regulatory Solutions.
Hostrin offers the following services:
1.In and out licensing Dossiers
2.Dossiers in CTD/ACTD/eCTD formats with e-softwares.
3.BE & Clinical studies Studies
4.CDMO (Contract Research & Development)
5.Tech transfer support and registration of dossiers in all markets.
6.Computer System Validations (CSV) as per GAMP 5 Guidelines, PLC/SCADA/HMI Validation, and Documentation.
7.Pharmacovigilance —Green Field projects
—CSV and Calibration
—Technology Transfer
—PDE & OEL
—Genotox Assessment of Impurity
—Gap assessment auidits
—Vendor audits
Pls visit our website www.hostringlobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
Mobile/
WhatsApp: +919949930343
marketing@hengkangpharm.cn
Zhejiang Hengkang group is FDA, EUGMP, PMDA, ANVISA, MFDS, NMPA approved company. Specialized on manufacturing & supplying various intermediates, APIs, FDFs with high quality and documentaiton.
