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foramjjani@gmail.com
Hello,
Greetings for the day!
My name is Foram Jani.
Regulatory: I provide end to end product registration services like compiling a dossier ECTD format based on country-specific requirements as well as query resolution. I can also prepare DMF, PV, COA, FPS and all pharma technical documents.
HR: Employee data management, payroll management, HR-related activities.
Looking forward for a positive response. Request you to forward to those who may have the above requirement.
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
ryanlyu-us@hnpoly.com
Hi, This is Ryan from Hainan Poly Pharm Co Ltd, we have the ability to be your CMO for your product. Our facilities are EU GMP and US FDA inspected. With huge available capacity left for your products. My phone number is also my whats app number,please feel free to call me.
the dosage form that we can manufacture(injections, tablets, capsules, dry suspensions, oral solutions, eye drops prefilled syringes, and topical ointments?
claudio.sepulveda@synthon.com
We are interested to be a CMO for pre filled syringes. Production in Chile. Authorize by EMA to export to EU.
