25 Jan 2023

Reply

Oseltamivir (75 mg) Tablets needed in Saudi Arabia [ENA16212]
A pharmacy that deals in the marketing & distribution of various finished dosage formulations is looking for suppliers of Oseltamivir (75 mg) Tablets for commercial purposes. The required quantity is 75,000 units.

Comments :

chowdary@carbontree.in

Dear Sir,

We can supply Oseltamavir 75mg tablets from our WHOGMP/ANVISA facility

17:26,  25 Jan 2023

khaitanavijeet@gmail.com

we can supply this.
please contact at +65 96799705

22:31,  25 Jan 2023

namrata.sutphinrx@gmail.com

Sutphin Drugs Inc are licensed distributors of USFDA approved RLD’s,(Branded & Generic) Drug Products including controlled (Narcotic / Psychotropic) products sold in the United States.

13:00,  27 Jan 2023

info@aeqpharma.com

We can support on pellets and tablet

14:22,  27 Jan 2023

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

11:59,  29 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

07:33,  30 Jan 2023
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