13 Jan 2023

Reply

Tender// Various Finished Dosage Formulations needed in Macedonia [ENA16074]
Public Health Institution General Hospital with extended activity Gevgelija is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 20-Jan-2023.
1. Famotidine (20 mg) Powder for Solution for Injections. The required quantity is 14,000 units.
2. Ascorbic Acid (500 mg/ 5 ml) Solution for Injections. The required quantity is 18,000 units.

Comments :

bd@revapharma.com

DEAR WE HAVE THE PROJECT.

KINDLY SHARE YOUR MAIL ID FOR SENDING THE DETAIL

11:32,  13 Jan 2023

bd@revapharma.com

DEAR WE HAVE THE PROJECT.

KINDLY SHARE YOUR MAIL ID FOR SENDING THE DETAIL

11:32,  13 Jan 2023

bd@revapharma.com

DEAR WE HAVE THE PROJECT.

KINDLY SHARE YOUR MAIL ID FOR SENDING THE DETAIL

11:33,  13 Jan 2023

bd@revapharma.com

DEAR WE HAVE THE PROJECT.

KINDLY SHARE YOUR MAIL ID FOR SENDING THE DETAIL

11:33,  13 Jan 2023

bd@revapharma.com

DEAR WE HAVE THE PROJECT.

KINDLY SHARE YOUR MAIL ID FOR SENDING THE DETAIL

11:33,  13 Jan 2023

export_commercial@bdpasargad.com

Dear Sir or Madam

We are excited to introduce to you, our company .
I’m writing to introduce our company BD Pasargad ,trading company in the field of finished dosage
We are currently exporting medicine to many countries.
We can prepare pharmaceutical products (tablet , capsule , ampule , prefilled syringe ,… ) in best price , we can support GMP , DMF or CTD for Registration .

Thanks, and best regards

Mohamad Norouzi
BD Pasargad
Mob : +989397665038

10:28,  14 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

12:39,  14 Jan 2023
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