02 Dec 2022

Reply

Capecitabine (150 mg & 500 mg) Tablets needed in Spain [ENA15720]
A company based in Switzerland that provides consultancy services to the pharmaceutical industry is looking for suppliers of Capecitabine (150 mg & 500 mg) Tablets for commercial purposes. The suppliers must support this enquiry with CEP & EU-MA.
1. Capecitabine (150 mg) Tablets. The required quantity is 3 lakh units for first year, 4 lakh units for second & third year and 5 lakh units for fourth & fifth year.
2. Capecitabine (500 mg) Tablets. The required quantity is 2.4 million units for first year, 2.5 million units for second year, 2.8 million units for third year, 3.2 million units for fourth & 3.5 million units for fifth year.

Comments :

chowdary@carbontree.in

Dear Sir,

We can supply Capacitabine 150mg & 500mg from our EUGMP facility. Our facility has been approved EUGMP, UKMHRA, Belarus, Korea, WHOGMP and PICs.

Please contact for more information

bd@spaccurelabs.com
www.spaccurelabs.com

20:44,  02 Dec 2022

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

12:45,  03 Dec 2022

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

12:45,  03 Dec 2022

chowdary@carbontree.in

Dear Sir,

We do supply both Capecitabine (500 mg & 150 mg) Tablets & Imatinib (100 mg & 400 mg) Tablets from our EUGMP facility. We have exclusive Oncology FDF manufacturing facility with EUGMP, Korean GMP, WHOGMP, PICs approvals, Belarus, Mexico and UKMHRA approvals. Please feel free to share your enquiry with quantity requirements and please visit our website for more information

Regards
PA Chowdary
bd@spaccurelabs.com
www.spaccurelabs.com

17:37,  03 Dec 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

07:39,  04 Dec 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

06:50,  05 Dec 2022

kaushal@newedgeoverseas.com

Please connect

12:00,  20 Dec 2022
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