Market Place
Reply
Comments :
himali.pawaskar@dksh.com
Hi, Please share this lead
pharmahouse@ymail.com
Services offered by PHARMA HOUSE
Dossiers (CTD, e-CTD, ANDA and ANVISA)
(All Country Specific, As per client request)
DMFs(CTD, e-CTD)(Open &Closed part)
(All Regions and Country regulations)
Technology transfers(API'S &Formulations),
( Paper technology & Product Development)
Pharmacovigilance(PV),
Intellectual properties(IP)
We have seperate Teams for Product Development for API'S &Formulations.
All product Documentations (Process, training, trouble shooting)
&other Regulatory services
Pharma House,
What's App & Voice:+91 81433 69525
pharmahouse@ymail.com ,
Hyderabad, India
info@auroscientific.in
Yes we can supply
info@auroscientific.in
Yes we can supply
harshad.solanki@apotheconpharma.com
We have USFDA and UK MHRA approved plant for API and finished formulation products.
hostrinlifesciences@gmail.com
Dear friend,
Greetings from Hostrin Life Sciences!!!
We have been supporting the following services.
1.We do support Tech transfer and Dossiers for Pharmaceutical, Biopharmaceutical, Nutraceutical, Biotech and Biosimilars in CTD, eCTD, ACTD, ANDA. DMF's for API's, Tech transfer support and Registration of Dossiers in MOH /MHRA/EMEA/FDA with 5 modules including BA and BE studies /Clinical studies/trials for finished formulation's in Pharmaceutical, ayurveda, Biotech, Biosimilar, vitamins , Peptides and Transdermal patches too.
2. eCTD publishing with potential software, addressing post submission queries from all regulatory authorities and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.
3. Impurity's & Reference standards support for API's
4. Services for IPR & Regulatory compliance
5. 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.
6. Custom synthesis and contract manufacturing services
7. Synthetic Resins technologies support.
8. Cleaning validation/ toxicology studies reports (PD values) for commercial manufacturing of APIs and finished formulations.
9. Pharmacovigilance services.
Pls don't hesitate to send your inquiries. 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
a.izadi@pharmanova.ae
Dear Sir/Madam,
I hope everything is well on your side.
PharmaNova is a wholesaler pharmaceutical raw material company and located in Dubai UAE with branches in Turkey, India and Hong Kong. We are providing top quality pharmaceutical raw material worldwide. We have very good network within China, India and Europe to support our customers worldwide from certified and regulated API and Excipients manufacturers, audited by international MOHs.
We are able to support you with this inquiry from certified source.
Best regards,
Ashkan Izadi
Business Development Specialist
Head Office:
Level 23 - Boulevard Plaza Tower 2
Emaar Boulevard, Dubai – UAE 124342
Cell: +971 52350 0672
Tel: +971 4 409 6859
FAX: +971 4 409 6850
www.pharmanova.ae
himali.pawaskar@dksh.com
Hi, Please share this lead
