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dieterschneider1703@gmail.com
EU based company (GMP, FDA inspected) is looking for such cooperations. Please contact us.
s.kapadiya@globi-corp.com
We can help to identify such manufacturers through our wide network in EU, India and Asia having EU-GMP and USFDA credentials for their plants, let us know more details by email.
vijaya.nuty@gvkbio.com
Our manufacturing facility has approvals from worldwide regulatory authorities like below and these accreditations facilitate faster and easier approvals of DMFs/dossiers for our business partners.
a) In rare instance a joint audit was performed by auditors from USFDA, EDQM and Spanish MOH in 2013.
b) We are approved by PMDA (Pharmaceutical and Medical Devices Agency) Japan in 2012 and supplying commercially to customers in Japan including Pfizer Japan.
c) FDA Korea approved us in 2012, we have our presence for a decade in Korea market and we serve to almost 8-9 OEMs.
d) USFDA in 2015 & 2018 (Received EIR)
p.hollanders@basicpharma.nl
We can help you with this product!
Please contact:
Peter Hollanders
BD Manager Basic Pharma p.hollanders@basicpharma.nl
hostrinlifesciences@gmail.com
Hii,
Greetings from Hostrin life Sciences !!!
We do support for the CMO & ANDA filing in USA,CTD,ACTD registration in MHRA/EMEA/MOH for Europe,UK,MENA,ROW market.
We do support with all modules including BE studies,Clinical studies for Lyphilized products, pharmaceuticals,Biotech,Biosimilars,Peptides,Transdermal Patches,Vitamins too.
Please go through our website: www.hostringlobal.com.
Looking forward to hear for your concerns,
Best Regards,
Andrew P
CEO & MD,
Hostrin Life Sciences,
andrew@hostringlobal.com
hostrinlifesciences@gmail.com
