Reply
1. Pamidronic Acid (15 mg/ ml) Injections. The required quantity is 50 units.
2. Cisplatin (1 mg/ ml) Injections. The required quantity is 100 units.
pharmahouse@ymail.com
We will supply, please let us know quantity required.
Pharma House,
pharmahouse@ymail.com
What's App & Voice:+91 8143369525
India.
chowdary@carbontree.in
We can supply Cisplatin 1mg/ml from our EUGMP certified facility. We have exclusive Oncology FDF manufacturing facility with EUGMP, MHRA, Korean GMP, WHOGMP and PICs approvals, more than 300 products are available with eCTD dossiers,
Regards
bd@spaccurelabs.com
www.spaccurelabs.com
enquiry@healthbiotech.in
Hello There,
Greetings from Health Biotech Limited!
We are one of the leading Indian Pharmaceutical Manufacturer & Exporter of finished formulations.Our state-of-the-art, WHO-GMP certified manufacturing
facilities are located in the industrial town of Baddi, in the State of Himachal Pradesh, India.
We are a global exporter and kindly contact us +91 987-688-2973 or send email enquiry@healthbiotech.in
Thanks,
Jay
Health Biotech Limited
www.healthbiotech.in
smit@salvavidaspharma.com
Hello
Myself Smit Jariwala from Salvavidas Pharmaceutical Ltd. I'm an international business executive.
We are the manufacturers and it can be available with us.
can we connect for some business?
Please, contact
smit@salvavidaspharma.com
Mo: +91 74359 19702 (Whatsapp : https://wa.link/8hjiee )
(Telegram : https://t.me/smit_slavavidas )
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
For all supply related queries like API, Intermediates, Finished Formulations please visit our website www.cristoneglobal.com
Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343
