17 Mar 2023

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Various Finished Dosage Formulations needed in Kazakhstan [ENA16638]
A company based in Switzerland that provides consultancy services to the pharmaceutical industry is looking for suppliers of Various Finished Formulations for commercial purposes. The required quantity is 24,000 units for each.
1. Tramadol HCl (100 mg & 200 mg) Capsules
2. Pregabalin (150 mg & 300 mg) Capsules

Comments :

namrata.sutphinrx@gmail.com

Sutphin Drugs Inc are licensed distributors of USFDA approved Reference Listed Drugs (RLD’s) ,Branded & Generic & Comparator Drug Products.
Kindly contact at info@sutphinrld.com or sutphinrx@gmail.com

18:54,  17 Mar 2023

info@indeximinternational.com

INDEXIM INTERNATIONAL, one of the leading manufacturer, suppliers, exporter and importer of API, Pharmaceutical formulation, Novel molecule, APIs, Vet.-APIs, reference standard, Impurities, Excipients, Intermediates, Solvents, Vitamins, Nutraceuticals and Dietary supplements, silica gel, Regulatory documents service etc.
We are exporting several of our products to Latin American countries, Gulf & Asian, Ukraine, Russia, and also a few products to Australia, UK & USA.
We are also contract manufacturer of APIs and attached is the list of products and by cooperation with other manufacturers in India. Also, most of the products are from WHO cGMP, ISO, GMP manufacturers.
sales.indeximinternational@gmail.com
info@indeximinternational.com
www.indexim.in
GSTN-24AADFI5767R1ZO
IEC -CODE : 0811024407
FDA No- 20B-168327/21B-168328
ISO 9000 AND GMP APPROVED

16:08,  18 Mar 2023

info@aeqpharma.com

contacy us

13:41,  20 Mar 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

07:18,  21 Mar 2023

j.hofmann@emergee.ch

Hello,
it's a pleasure to introduce our company's profile and services.
We are a Swiss wholesale (GDP certified) pharmaceutical company. We work ONLY with validated suppliers, fully licensed by the Health Authorities. Our suppliers are Swiss/EU manufactures, wholesalers located in Europe, USA, Asia, Canada, and many other countries.
Please get in touch if you're interested.
I look forward hearing from you!
BR
Jeanette Hofmann

12:27,  28 Mar 2023
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