13 Aug 2022

Reply

Tender// Adalimumab Injections needed in Czech Republic [ENA14682]
University Hospital Vinohrady is looking for supplies of Adalimumab (40 mg/ 0.4 ml or 80 mg/ 0.8 ml) Injections for commercial purpose. The required quantity is 6,800 units & 30 units respectively. The deadline is 25-Aug-2022.

Comments :

chowdary@carbontree.in

Dear Sir,
We do supply Adalimumab 40mg PFS in 45days for 6800 units from WHOGMP certified facility. COA, WHOGMP, FSC, Licence copy and Art work will be provide.

18:04,  14 Aug 2022

chowdary@carbontree.in

Dear Sir,

Small quantity 38units will be supply before 25th August. Remaining will be in 30-45days

18:28,  14 Aug 2022

Dear Sir/Madam,
I am writing on behalf of D's Healthcare Company. We may provide support to you. Can you please reach out to us if you have ongoing inquiries like this; we are eager to discuss supply base trade opportunities.
Best Regards.
Dr. Samican Dabanlioglu
00905305046075
samicand@dshealthcarecompany.com

14:58,  17 Aug 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

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

12:47,  02 Sep 2022

enquiry@healthbiotech.in

Hello There,

Greetings from Health Biotech Limited!

We are one of the leading Indian Pharmaceutical Manufacturer & Exporter of finished formulations.

Our state-of-the-art, WHO-GMP certified manufacturing facilities are located in the industrial town of Baddi, in the State of Himachal Pradesh, India. We are a global exporter and kindly contact us for the mentioned requirement.

Thanks,

Jay
Health Biotech Limited
+91 987-688-2973
enquiry@healthbiotech.in
www.healthbiotech.in

18:49,  07 Sep 2022
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