07 Nov 2022

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Tender// Various Finished Dosage Formulations needed in Poland [ENA15484]
Health Care Team in Strzyzow is looking for supplies of Various Finished Dosage Formulations for commercial purposes. The deadline is 1-Dec-2022.
1. Ceftazidime (1 g) Powder for Solution for Injections or Infusions. The required quantity is 2,100 units.
2. Methylprednisolone (40 mg) Injections. The required quantity is 750 units.

Comments :

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 form .
We are currently exporting medicine to many of countries .
We can prepare pharmaceutical products (tablet , capsule , ampule , prefilled syringe ,… ) in best price , we can support GMP , DMF or CTD for Registration .
For future queries as well as a sample and price , please do not hesitate to contact the undersigned .


Thanks, and best regards

Mohamad Norouzi
BD Pasargad
Mob : +989397665038
Tel : 021-88770144
www.bdpasargad.com
Address: Unit 4, Floor 2, No 354, Dastgerdi St,
Nelson Mandella (Jordan) Blvd , Tehran , Iran

12:39,  08 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

07:42,  11 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

07:12,  24 Nov 2022

petina@ananta.com.ua

Dear Sir,

Ananta Medicare Ltd owns 3 plants in India. We have offices in Ukraine, UK and India.
We manufacture Cephalosporins Injectables (Ceftriaxone, Cefepime, Ceftazidime, Cefoperazone etc.).
Our plant has PIC/S GMP issued by Ukraine. Products are registered in Ukraine. We can do supply from Ukraine or India.
Please contact me. Email:petina@ananta.com.ua

14:14,  30 Jan 2023
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