09 Jan 2023

Reply

Tender// Various Finished Dosage Formulations needed in Poland [ENA16034]
Szpital Uniwersytecki W Krakow is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 2-Feb-2023.
1. Darbepoetin Alfa (500 mcg/ ml) Solution for Injections. The required quantity is 1,600 units.
2. Aflibercept (40 mg/ ml) Solution for Injections. The required quantity is 900 units.

Comments :

chowdary@carbontree.in

Dear Sir,

We can supply Darbepoetin Alfa (500 mcg/ ml) Solution from WHOGMP facility, COPP, COA, License copy, ARTWORK, Packshot available

13:42,  09 Jan 2023

chowdary@carbontree.in

Dear Sir,
We are producing Biosimillars from WHOGMP facility.

Brand/Product

Generic Name

Strengths

Presentation

DERISE

Darbepoetin Alfa

25mcg
40mcg
60mcg
100mcg
200 mcg
PFS


Rituximab
100 mg/10 mL &
500 mg/50 mL
Vial


Bevacizumab
100 mg/ 4 mL &
500 mg/ 16 mL
Vial


Adalimumab
10 mg/ 0.2 mL
20 mg/ 0.4 mL
40mg/ 0.8 mL
PFS



Trastuzumab
150mg / 440mg
Vial + Dilu

08:55,  10 Jan 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

09:14,  11 Jan 2023
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