Regulatory Affairs we are Specialists in obtaining and maintaining government approval for drugs, medical devices, nutritional products, and related materials. Part of our strategic guidelines is to strike a balance between regulatory concerns, technology, marketing objectives, compliance, time to market and costs.
In order to place your product in the Latin America market, a registration and approval with the regulatory departments required. We can offer you a full service of regulatory affairs. We offer the ability to market your product in Latin America with the speed necessary for you to see profits quickly by designating UNO HEALTHCARE as the Latin America Registration Holder.
· Hold your registration approval.
· regulatory departments relationship
· Registration process
· Logistics http://www.cjlexpress.com/
Uno Healthcare has knowledgeable staff with expertise in providing an exchange of product safety information in order to meet regulatory requirements with the health authorities. We prepare action plans in order to minimize any risks that our partners might incur, including patient registry requirements. We facilitate identification of any new and emerging product safety issues on an ongoing basis.