17 Nov 2022

Reply

Tender// Cetuximab Solution for Infusions needed in the Czech Republic [ENA15578]
Krajska nemocnice Liberec, AS is looking for supplies of Cetuximab (5 mg/ ml in 20 ml) Solution for Infusions for commercial purposes. The required quantity is 1,066 units. The deadline is 13-Dec-2022.

Comments :

chowdary@carbontree.in

Dear Sir,

We can supply Cetuximab 5mg/ml in 20ml along with COA, Artwork, Packshot, COPP, WHOGMP, FSC, license copy, lead time will be 45-60days for 1000-3000vials

13:31,  17 Nov 2022

chowdary@carbontree.in

Dear Sir,

We can supply Cetuximab 5mg/ml in 20ml along with COA, Artwork, Packshot, COPP, WHOGMP, FSC, license copy, lead time will be 45-60days for 1000-3000vials

We have ready stocks Adalimumab 40mg PFS 5000vials, Bevasizumab 400mg 5500vials and Infliximab 100mg 3000vials.

Please feel free to send enquiry for documents.

Regards
PA Chowdary

13:34,  17 Nov 2022

hostrinlifesciences@gmail.com

Dear friend,

Greetings from Hostrin Life Sciences!!!

We have been supporting 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 and all type of mock audits like USFDA_21_CFR with GAP filling for USFDA, WHO-GMP, EU-GMP, MHRA, TGA, PMDA and PICS audits as well.

3. Impurity's & Reference standards support for API's

4. Services for IPR & Regulatory compliance

5. 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.

6. Custom synthesis and contract manufacturing services

7. Synthetic Resins technologies support.

8. Cleaning validation/ toxicology studies reports (PD 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

21:18,  17 Nov 2022

gitika@kwalitypharma.com

Good day!!
we will be able to fulfil the requirement ,but lead time is 40 to 60 days.other biosimilars are also available.kindly approach or contact
Ms.geetika Arora(chief executive)
e-mail-gitika@kwalitypharma.com
phone-+91-8527646355

11:59,  19 Nov 2022

dep5@techemi.com

Anhui Sinotech industrial co.,ltd one of the leading manufacturer, suppliers of API, Vet.-APIs,.We supply the APIS and documents. The goods is origin China .We can supply the COA and the goods package.. Please contact us : Xu ping

Anhui Sinotech Industrial Co.,Ltd
Tel: 86-551-65692531
Whatsapp/Mob: 0086-13866721542
Email: dep5@techemi.com
Web: http://www.techemi.com

07:32,  22 Nov 2022

dep5@techemi.com

Anhui Sinotech industrial co.,ltd one of the leading manufacturer, suppliers of API, Vet.-APIs,.We supply the APIS and documents. The goods is origin China .We can supply the COA and the goods package.. Please contact us : Xu ping

Anhui Sinotech Industrial Co.,Ltd
Tel: 86-551-65692531
Whatsapp/Mob: 0086-13866721542
Email: dep5@techemi.com
Web: http://www.techemi.com

07:32,  22 Nov 2022
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