Reply
pharmahouse@ymai.com
We are providing below services required people contact privately.
Dossiers (CTD, e-CTD, ANDA and ANVISA)
DMFs(CTD, e-CTD)
Technology transfers(API'S &Formulations),
Pharmacovigilance(PV),
Intellectual properties(IP)
Product Development for API'S &Formulations.
&other Regulatory services.
Pharma House,
pharmahouse@ymail.com ,
Hyderabad, India
Whats App&Voice:+91 7799500435
smatam81@gmail.com
Hi,
Greetings from Veerab Pharma Products limited,
We are pleased to inform you that we can support your products. Kindly share your contact details on our email to proceed further
Regards
Santhosh
info@indeximinternational.com
we are one of the leading supplier, exporter and importer of Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, industrial Chemicals, Excipients, Ingredients, Drug Intermediates, Pharmaceutical pellets, probiotics, enzyme, Solvents, Phytochemicals, Extracts, Food & Feed Additives, Vitamins, Nutraceuticals and Dietary supplements etc.
We are exporting several of our products to Latin American countries, Gulf & Asian countries and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India . Also most of the products are from WHO cGMP , ISO , GMP manufacturers.
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 ROW/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
bd@ahslifesciences.com
We can provide the EUCTD dossier
pharmatechhng@gmail.com
Dear Sir / Madam,
Greetings from PHARMATECHH , INDIA
PHARMATECHH is a marketing firm engaged for the export of Food Ingredients , Pharma finished formulations, domestic formulations products, Indian FDA approvals of mfg. sites and also up gradation of formulation units.
We have various export business under execution,to name a few :
a. Lyophilised Injections for a company based in Egypt .
b. e CTD Dossiers for an Australia based company.
c. Ointments for an Australian company etc.
In addition to above, we have an exclusive tie-up with a full fledged API's / Intermediaries / Excipients / Food Ingredients manufacturers for marketing & sale of their products.
If you are importing any API / Excipients / FOOD Ingredients then please let us know your requirements. We will discuss your requirements with our Indian and Chinese manufactures and offer you quality product at best available price.
Please let us know your requirements of Ceftriazone Sodium along with packing details and your target price.
Let us explore possibilities of business which will be beneficial to both our companies. Kindly request you to share purchase division email id.
Looking forward to your kind response.
Regards,
Milind M. Sawant
Pharmatechh NextGen Services
New Mumbai - India
Whatsapp:+91-9223237213 WeChat: sawantmilind
pharmatechhng@gmail.com
www.pharmatechhng.webs.com
export@healthpharma.in
Dear Sir,
Greetings from Health Pharma...!!!
For your ready reference we have Ready dossier list more than 1000 formulations, 300 ANDA, 50 Monoclonal Antibodies Dossiers, 260 EU GMP Approvde dossier, 80 MA trasnfer Dossier application, 2500 Open Part DMF, 150 Close part DMF, ready AMV, country specific dossier, All of them are open for the Technology transfer.
Kindly request you to send an email for further discussion.
Thanks..!!!
g.rossi@phshop.it
Good day, I am Gennaro Rossi, sales manager of PhShop (www.phshop.it), we are a Italian pharmaceutical wholesaler and
we can provide you what you are looking for
Please contact me for further details
Best regards
Gennaro Rossi
