Advising a major manufacturer of pharmaceuticals on product life cycle management

Advising a major manufacturer of pharmaceuticals on product life cycle management (ensuring RDP of innovative medical products against generic product applications, FOI requests with State Agency of Medicines, appealing State Agency of Medicines decisions in Ministry of Health), as well as advice regarding pharmaceutical/medical event sponsorship, donations and contributions to health professionals and associations, educational speakers agreements; clinical trial agreements, etc. review and comment internal compliance policies to avoid conflict of interest issues; advice regarding distribution of free samples of medication, donation of medications to hospitals (Latvia)