27 Oct 2023

Reply

Tender// Various Finished Dosage Formulations needed in Bulgaria [ENA18461]
Complex Oncology Center - Ruse Ltd is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 23-Nov-2023.
1. Capecitabine (500 mg) Film Coated Tablets. The required quantity is 57,600 units.
2. Imatinib (100 mg) Film Coated Tablets. The required quantity is 14,600 units.

Comments :

export1@pranadabiopharma.com

Hello! Greetings from Pranada Biopharma Pvt. Ltd. We can supply your required Products at the best rate. Please contact us at export1@pranadabiopharma.com for more details.

13:32,  27 Oct 2023

sales1@vivindrugs.com

Dear Sir,

We can supply below products from our WHOGMP/EUGMP facility

1.Capecitabine (500 mg) Film Coated Tablets. The required quantity is 57,600 units.
Lead time. 3-4weeks

2. Imatinib (100 mg) Film Coated Tablets. The required quantity is 14,600 units.
Lead time. 3-4 weeks

17:58,  27 Oct 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 formats. DMF support for API's as well.

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 softwares like Lorenz/Docubridge/PharmaReady/E-Way addressing post submission queries from all regulatory authorities.

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

4. Services for IPR & Regulatory compliance with all risk assessments.

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.

7. Custom synthesis, contract manufacturing services and conducting BE studies and clinical studies from US-FDA,EU-GMP, UK-MHRA, TGA-Australia approved CRO's/BE Study Centers.

8. Synthetic Resin technologies support.

9. Cleaning validation/ toxicology studies reports (PDE/ADE I OEL) values for commercial manufacturing of APIs and finished formulations.

10. 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
www.hostringlobal.com

13:48,  31 Oct 2023

xueqihuang@southpharma.com

Dear Sir/Mrs,
We are a professional pharmaceutical manufacturer from Fujian, China. The Imatinib tablet(100mg) you are looking for is one of our product and it has passed local GMP audit.
Welcome to contact me for more details through xueqihuang@southpharma.com and +8618659155504(wechat/whatsapp)
Regards, Qihuang

12:55,  16 Nov 2023

xueqihuang@southpharma.com

Dear Sir/Mrs,
We are a professional pharmaceutical manufacturer from Fujian, China. The Imatinib tablet(100mg) you are looking for is one of our product and it has passed local GMP audit.
Welcome to contact me for more details through xueqihuang@southpharma.com and +8618659155504(wechat/whatsapp)
Regards, Qihuang

12:55,  16 Nov 2023
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