08 Nov 2024

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Various Finished Dosage Formulations needed in India [ENA21064]
A company that focuses on distribution of various finished formulations is looking for suppliers of various finished dosage formulations for commercial purposes. The suppliers must support this enquiry with ACTD dossier and GMP. The required quantity is 300,000 units in first year, 345,000 units in second year and 410,000 units in third year for each. The final market is Singapore, Malaysia, Hong Kong, Philippines and Vietnam.
1. Atropine (0.01%, 0.025%, 0.05%) Eye Drops
2. Pilocarpine (1.25% or 2%) Eye Drops

Comments :

foramjjani@gmail.com

Greetings for the day!
My name is Foram Jani from Mumbai, India. I can arrange DMF, dossiers & regulatory documents.
Whtsapp: +919819435009

15:10,  08 Nov 2024

vishvesh.shaishav@gmail.com

We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108

20:24,  08 Nov 2024

vishvesh.shaishav@gmail.com

We are focussed on developing new manufacturing technologies, including custom synthesis of new moleculepharma intermediate, catalyst, bulk drugs, pharma API, pharma chemicals, active pharmaceutical ingredients, pharmaceutical pellets,additives, contract manufacturing, chemicals. We began in the field of specialty intermediates for pharmaceutical applications and developed our own purification technologies for manufacturing highly pure intermediates. And Pharmaceutical API At a later stage, we integrated forward to manufacture finished formulations for both veterinary and human consumption. Due to our completely integrated operations in the pharmaceutical sector, we continuously learn about the quality parameters for an API based on the performance of the finished formulation in order to quality their Bioequivalence Studies.?We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.?Our focus lies in developing new production technologies with a keen interest in frugal innovation in order to gain a competitive edge over others. We specialize in the custom synthesis of molecules and work with many reputed companies around the world on an OEM basis.pharmaceutical pellets,Intermidiates ?Our finished formulations from WHO-GMP and EU-GMP units are registered/being registered in 26 countries within Asia, Europe, North America, Latin America and Africa continents including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad, Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.?vishvesh.shaishav@gmail.com
+919725487108
+919726387108

20:27,  08 Nov 2024

Kishore@jacksonlaboratories.com

Hi please contact Kishore@jacksonlaboratories.com ,We have our own WHO certified manufacturing unit

12:36,  09 Nov 2024

export3@neha-chemicals.com

"Dear sir
We do supply best quality and best price and intime supply

14:34,  25 Nov 2024

bd@aizant.com

Aizant Drug Research Solutions is a leading GMP-certified CMO specializing in the manufacturing of various dosage forms, including Sterile Injectables, Nasal, Topical, Solid Dosage, and Liquid formulations. With extensive expertise and state-of-the-art facilities, Aizant ensures high-quality production and compliance, offering end-to-end solutions from development to commercial manufacturing.

Contact us at bd@aizant.com.

09:39,  26 Nov 2024

SALES@GABANETICPHARMA.COM

WE HAVE IN HOUCE REGULATORY TEAM TO SUPPORT ALL DOCUMENTORY SUPPORT FOR EXPORT KINDLY CONTACT US AT SALES@GABANETICPHARMA.COM

12:15,  30 Nov 2024
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