13 May 2022

Reply

Ketorolac Tromethamine API needed in Belarus [ENA13622]
A largest company that specializes in the development and implementation of new pharmaceutical products is looking for suppliers of Ketorolac Tromethamine API for commercial purpose.

Comments :

luisa.goglia@fischer-group.ch

Dear All,
please contact Fischer Chemicals AG in Switzerland. Thank.

12:40,  13 May 2022

info@aeqpharma.com

we supply Ketorolac Tromethamine with full docs, DMF,gmp..
info@aeqpharma.com

13:30,  13 May 2022

arunodayalabs@gmail.com

We are the largest manufacturers for Ketorolac tromethamine USP/EP from WHOGMP certified facility with DMF.

13:36,  13 May 2022

harshad.solanki@apotheconpharma.com

"Greetings for the day !

I take this opportunity to write to you with introduction of Apothecon Pharmaceuticals P. Ltd.

Apothecon Pharmaceuticals established in year 2007 and Apothecon have valid approval like US-FDA, UK-MHRA, Anvisa, TGA, WHO-GMP Etc.

Apothecon offer API, Intermediates and FDF products from Regulatory approved plant.
"

14:49,  13 May 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

17:47,  13 May 2022

Crystalchemicalsfzllc@gmail.com

Dear Friend,

Please contact on the following emails for quotation.

Thanks and Regards,

Dr. Amna Nawaz
CRYSTAL CHEMICALS FZ-LLC - UAE -|- China -|- Pakistan
M: +92-321-8444610 (Whatsapp)
Skype: Crystalchemicals786
E: import@crystalchemicals.com.pk, Crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk

13:56,  14 May 2022

a.izadi@pharmanova.ae

Dear Sir/Madam,

I hope everything is well on your side.

PharmaNova is a wholesaler pharmaceutical raw material company and located in Dubai UAE with branches in Turkey, India and Hong Kong. We are providing top quality pharmaceutical raw material worldwide. We have very good network within China, India and Europe to support our customers worldwide from certified and regulated API and Excipients manufacturers, audited by international MOHs.

We are able to support you with this inquiry from certified source.

Best regards,

Ashkan Izadi
Business Development Specialist
Cell: +971 52350 0672
Tel: +971 4 409 6859
FAX: +971 4 409 6850
www.pharmanova.ae

16:52,  16 May 2022

heliantus@heliantus-milano.it

Dear Sirs,

We can offer you said API. Can you contact HELIANTUS SRL, in Italy.
Our mail are:

marco_sgaravatti@hotmail.com
heliantus@heliantus-milano.it

Thank you & bst regards

Marco

02:02,  17 May 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

Best Regards,
Andrew P
CEO & Managing Director
Hostrin Life sciences
hostrinlifesciences@gmail.com
andrew@hostringlobal.com
Mobile/
WhatsApp: +91 9949930343

22:14,  17 May 2022

sam.d@micoson.com

We will provide timely quotes and documentation support, please send an email to sam.d@micoson.com.
Thank you.

10:09,  20 May 2022

alicechan@huarizy.com

HUNAN HUARI PHARMACEUTICAL CO.,LTD. is the Chinese manufacturer for the following APIs and excipients, please feel free to contact us if you have any requirements.

1) Citric acid Monohydrate GMP
2) Citric acid Anhydrous GMP
3) Sodium citrate GMP
4) Potassium Citrate GMP
5) Sodium benzoate
6) Stearic acid
7) Sodium cyclamate
8) Potassium Sorbate
9) Polysorbate 80

email address: alicechan@huarizy.com
phone number: +86 18820220687

07:13,  23 May 2022
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