10 Apr 2023

Reply

Tender// Rituximab Concentrate for Solution for Infusions needed in Belgium [ENA16846]
MercurHosp ASBL is looking for supplies of Rituximab (100 mg) Concentrate for Solution for Infusions for commercial purposes. The required quantity is 1,762 units. The deadline is 12-May-2023.

Comments :

chowdary@carbontree.in

Dear Sir,

We can supply Rituximab (100 mg) Concentrate for Solution for Infusions in 3-4weeks from our WHOGMP facility.
COA
Artwork
COPP/Free sale certificate
Pack insert
License copy will be arrange for approval.
We have ready dossier and clinical data for Rituximab.

Adalimumab, Bevasizumab, Rituximab, Trastuzumab, Pembrolizumab, Nivolumab, Infliximab, Cetuximab, Denosumab, Pertuzumab, Darbopoetin Alfa B, Erythropoietin, Teriparatide, L-Asperginase, Pegaspergase, Goreselin, Leuprolide and 200 oncology products are our manufacturing products.

Best Regards
PA Chowdary
arunodayalabs@gmail.com

10:43,  10 Apr 2023

graham.ashton@activepharma.co.uk

We manufacture this product

14:35,  12 Apr 2023

graham.ashton@activepharma.co.uk

We manufacture this product

14:35,  12 Apr 2023

graham.ashton@activepharma.co.uk

We manufacture this product

14:35,  12 Apr 2023

hostrinlifesciences@gmail.com

Dear Friend,

Greetings from Hostrin Life Sciences!!!

Hostrin offers 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.

3. Support for Impurity's, Reference standards and RLD's

4. Services for IPR & Regulatory compliance

5. Services for Quality Management Systems: GXP/GMP Advisory & EU-GMP/UK-MHRA/TGA/PMDA/WHO-GMP/PICS and USFDA_21_CFR with all GAP filling Audits.

6.Supporting for QBD - SIGMA TECH Software version 3.1 for DOE, Robustness for the R&D in Pharma, Biotech, Biosimilars manufacturers to save the time and cost effective technology.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) 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

07:58,  13 Apr 2023
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