04 Jul 2022

Reply

Various APIs needed in Peru [ENA14194]
A company that focuses in manufacturing of finished dosage formulations is looking for suppliers of Various APIs for development purpose. The suppliers must support this enquiry with CoA.
1. Prostaglandin (0.5 g) API
2. Papaverine (250 g) API
3. Chlorpromazine (10 g) API
4. Atropine (2 g) API
5. Etilefrine (50 g) API
6. Phentolamine (20 g) API

Comments :

SALVAVIDAS PHARMACEUTICAL PVT.LTD

We are A Reputed Pharmaceutical Product manufacturer, Exporter, and Export of various types of Pharmaceutical Products throughout the world.

We are dealing in Active Pharmaceutical Ingredients (API’s), Veterinary APIs, Intermediates, Excipients & Chemicals… We deal with Branded Drugs along with all Related Documents and Certificates.

We have a wide range of Medicines like Antibiotics, Cardio diabetics, Anti-Cancer, Nutraceuticals & Many more.

We are always there to serve you with our best services

All Products are Manufactured in WHO, GMP, ISO 9001 certified manufacturing units.

Best Regard.
Rohan Patel
Business Development Executive
Email- rohan@salvavidaspharma.com
Whatsaap- +91-9313237877
Web: www.salvavidaspharmaceutical.com

10:37,  04 Jul 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 APPROVE

10:55,  04 Jul 2022

navee@chemyzolab.com

Dear sir,
please write your requirements to navee@chemyzolab.com

12:03,  04 Jul 2022

crystalchemicalsfzllc@gmail.com

We can supply the following API, Please contact

Crystal Chemicals FZ-LLC
FDRK-3517, PO Box # 10055, Ras-AL-Khaimah, United Arab Emirates
Mobile & (Whatsapp) +92-333-8484130
E: crystalchemicalsfzllc@gmail.com
W: www.crystalchemicals.com.pk`

12:28,  04 Jul 2022

bdevomaar@gmail.com

Dear;
Please send on below email your inquiry.
We can support your requierment for the APIs with all documents for registration.
bdevomaar@gmail.com
Best regards.

13:22,  04 Jul 2022

sales6@iffect.com.cn

Greetings from Iffect Chemphar Co., Ltd!
IFFECT CHEMPHAR CO., LTD. is one of the biggest R&D and manufacturer base specialized in new and high valued added APIs in China, we are both manufacturer and exporter for Pharmaceuticals & Veterinary API and its main intermediates. And now we are on the way to apply for COS and FDA approval for some of our products. Meanwhile we are also willing to register our products in your market if it's requested.

We could supply
Prostaglandin USP
Chlorpromazine HCL BP
Atropine Sulfate USP
Etilefrine HCL EP
Phentolamine Mesylate USP
at any quantity.
More information needed, please feel free to contact.

14:57,  04 Jul 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

01:24,  10 Jul 2022

masahiro-aoki@katsura-chemical.co.jp

We,Katsura Chemical Co.,Ltd., are Atropine Sulphate hydrate manufacturer in Japan. our Atropine has been supplying te market properly, having MasterFile in Japan, GMP as well. If you are still interesting Atropine for R&D purpose, please let me know. URL : https://www.katsura-chemical.co.jp/en/ contact : masahiro-aoki@katsura-chemical.co.jp tel : +81-46-251-0948

06:15,  22 Feb 2023
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