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1. Calcium Carbonate 500 mg Tablet (calcium equivalent to 200 mg)- Volume: 10 Million units
2. Colchicine 0.5 mg Tablet- Volume: 500,000 units
3. Allopurinol 300 mg Tablet- Volume: 10,000 Million units
4. Allopurinol 100 mg Tablet- Volume: 10,000 Million units
5. Mefenamic Acid 500 mg Tablet- Volume: 300 Million units
6. Mefenamic Acid 250 mg Capsule- Volume: 400 Million units
7. Chlorphenamine 4 mg Tablet- Volume: 10 Million units
8. Nitroglycerin Sublingual Tablet 0.5 mg (bottle pack of 10s can be considered)- Volume: 20 Million units
9. Cetirizine 10 mg Tablet- Volume: 1 Million units
10. Diclofenac SR 50 mg Tablet- Volume: 1 Million units
Suppliers must support with GMP from PIC/S country; Product dossier in CTD form; Stability Data Zone 4b.
Packaging requirement: Blister pack of 10s X 10 and 10s X100.
Comments :
gm@probitypvt.com
Hi,
Can you pls get ih touch to take this forward?
bd@ahslifesciences.com
Lets connect we can support with EUGMP products.
mspharmachem@gmail.com
Yes We Can Provide almost 90% of your requirement with CTD & EU GMP
marketing@baschamlifesciences.com
Greetings from Bascham Life Sciences
We are pleased to inform you that we can support this requirement. Kindly share your contact details on our email to proceed further
Regards
Bascham Team, India
export@healthpharma.in
Dear Sir,
Greetings from Health Pharma.
We can support you with PIC/s approved plant for the same. We request you to send your requirements through an email.
Thank you.
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 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
export@healthpharma.in
Dear sir,
Greetings from Health Pharma...!!!
We can support you with asked products. We request you to send us an email containing all information so we can act accordingly.
Your response is awaited.
Thank you...!!!
