Comments :
info@vidacurepharma.in
We can support Contract Development and Manufacture for all oral solid and liquid dosage form.
Please contact us at info@vidcaurepharma.in
9033821438
randy.eik@missionpharmacal.com
Mission Pharmacal is a privately held pharmaceutical company based in San Antonio, Texas that has expansive capabilities as a Contract Development and Manufacturing Organization (CDMO) for US and international clients. Mission Pharmacal’s advanced pharmaceutical manufacturing facilities feature 275,000 square feet of product and warehousing space. Using the latest high-capacity equipment, we produce gels, liquids, creams, and semi-solids, along with more than 1.5 billion tablets a year.
Packaging
Mission offers a full spectrum of printing and packaging capabilities based on customer’s needs. Our facilities are equipped with serialization capabilities in line with the U.S. regulatory requirements and today's introduction of the Drug Supply Chain Security Act (DSCSA).
www.missionpharmacal.com
I welcome an opportunity to further discuss our capabilities to meet your CDMO RX and/or OTC needs now or in the future. .
Please let me know if you have any interest and I will request a CDA to be prepared to begin discussions.
Thank you,
Randy Eik
VP, Contract Development & Manufacturing
randy.eik@missionpharmacal.com
Phone:800-373-3037 Ext 5505
Cell: 423-943-5120
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
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
Akansha.chauhan@apicore.com
We can support you on this. Kindly contact us for further details.
sumit@saappharma.com
Good afternoon,
Dear Sir.
We are OUT SOURCING Agency with several CDMO in our NETWORK for several HUNDRED products mfg in all Category.
We can deliver all products at best Price with Best QUALITY .
We have CDMO Having KENYA / TANZANIA / UGANDA/ and various other Country MOH approved.
pl contact us ;- sumit@saappharma.com
maria.rojas@vir.es
We can support Contract Development and Manufacture for all oral solid and liquid dosage form. https://vir.es/ (EU-GMP)
Please contact us at registro@vir.es
+34 914862990
akansha.chauhan@apicore.com
My self Akansha Chauhan, The Manager Of Sourcing and Procurement Department in APICORE PHARMACEUTICAL PVT. LTD.
• Short Introduction
Apicore Pharmaceutical Pvt. Ltd. is the subordinate of APICORE LLC (New Jersey 2003) , Commenced operations in 2006. Our company is in the group of RK PHARMA INC, In New York.
Our company leading process in APIs, Intermediates & Formulations manufacturing service provider for the worldwide pharmaceutical industry and to the distributors. We are GMP and 5 times USFDA inspected organization in india.
Kindly go through to our website www.apicore.com
www.rkpharmainc.com
akansha.chauhan@apicore.com
My self Akansha Chauhan, The Manager Of Sourcing and Procurement Department in APICORE PHARMACEUTICAL PVT. LTD.
• Short Introduction
Apicore Pharmaceutical Pvt. Ltd. is the subordinate of APICORE LLC (New Jersey 2003) , Commenced operations in 2006. Our company is in the group of RK PHARMA INC, In New York.
Our company leading process in APIs, Intermediates & Formulations manufacturing service provider for the worldwide pharmaceutical industry and to the distributors. We are GMP and 5 times USFDA inspected organization in india.
Kindly go through to our website www.apicore.com
www.rkpharmainc.com
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...!!!
Dear Sir,
We at Zenon can support you in your manufacturing requirements for suggested therapies from our manufacturing facility.
To discuss things ahead request you to kindly email your target portfolio and regulatory requirements on abhishek@zenonhealthcare.com
Abhishek Tulsyan
Director,
Zenon Healthcare Limited