16 Mar 2021

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Looking for a GMP approved CDMO to manufacture Bilayer Tablets [ENA09962]
A pharmaceutical manufacturing company that deals in lozenges, micro-effervescent, patches and sprays is looking for a GMP approved CDMO to manufacture Bilayer Oral Tablets (OTC). The packaging should be in PVC-PVDC/ Alu. The project launch time is 2024. The final market is Europe.

Comments :

zhang.chunlin@reyoung.com

Dear ,
This is Reyoung Pharma from China ,
please share more information,
Maybe we can offer ,
keep in touch

05:51,  18 Mar 2021

zhang.chunlin@reyoungh.com

Dear ,
This is Reyoung Pharma from China ,
please share more information,
Maybe we can offer ,
keep in touch

05:53,  18 Mar 2021

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

22:51,  19 Mar 2021

jgq@yangzijiang.com

jgq@yangzijiang.com

I am Justin from Yangtze River Pharmaceutical Group in China

APIs and FDF can be manufactured by our company.

We can also CMO

If you need them, please contact me by Tel., WhatsApp and Wechat: +86 15261051195
Email: jgq@yangzijiang.com

13:39,  27 Mar 2021

c.papadi@famar-group.com

we can support your request. please contact us

19:23,  20 Apr 2021

export@healthpharma.in


Dear Sir,

Greetings from Health Pharma...!!!

We can support you with your requirements. Kindly request you to send email for detailed information.

Looking forward to your positive response.

Thanks...!!!

18:22,  05 Jul 2021
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