20 Jun 2023

Reply

Tender// Various Finished Dosage Formulations needed in Poland [ENA17353]
Szpital Powiatowy w Chrzanowie is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 18-July-2023.
1. Abiraterone Acetate (500 mg) Tablets. The required quantity is 1,680 units.
2. Capecitabine (500 mg) Tablets. The required quantity is 12,600 units.

Comments :

arslan@risenchemicals.com

We can supply the same from our WHO/GMP USFDA approved sources,please revert via email or WhatsApp for more details.

Regards
Ali Arslan
WhatsApp: 00923214949909
Email: arslan@risenchemicals.com

14:34,  20 Jun 2023

sales1@vivindrugs.com

Dear Sir,

We shall supply from our WHOGMP & EUGMP facility

1. Abiraterone Acetate (500 mg) Tablets. The required quantity is 1,680 units.
Lead time. 3-4weeks

2. Capecitabine (500 mg) Tablets. The required quantity is 12,600 units.
Lead time. 3-4weeks

22:06,  20 Jun 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

01:39,  21 Jun 2023
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