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1. Regulatory support
 

1.1. Consulting and expert advising in the scope of establishment, development and implementation of the harmonized regulations for the scope of medicinal products manufacture and marketing.


1.2. Consulting and expert advising in the scope of establishment, development and implementation of the contemporary international regulations for the scope of controlled substances (toxins, pesticides, drug of abuse, narcotics, pollutants, etc.) manufacture, transporting, marketing and waste disposal.


1.3. Consulting activities intended to support implementation of rational health economic approach to establishment or restructuring of health policy (registration, pricing, reimbursement, pharmacovigilance, etc.), including advising to re-organization and restructuring of health funds, establishing of lists of medicines, implementation of principles for the rational therapy and use of medicines.


1.4. Development and implementation of organization and information management systems in support to national regulatory activities.


 
 

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