DRA Consulting Oy specialises in consultation and management of marketing authorisations, price applications, pharmacovigilance, wholesale activities and marketing. We operate actively in the Nordic countries, and also Europe-wide.
Our regulatory intelligence teams will help you decide on the best strategies and ensure a smooth process from product development to market launch – always the fastest way.
Do you appreciate fast delivery of accurate translations and knowing your facts and figures are correct? Our medical translators are here to help you with all your language-related needs.
Expertise in wholesale activities guarantees product availability and rapid action in case of product defects.
Appropriate documentation is key to a successful application process and fast market access.
Can you get your marketing message across? We offer you an efficient process which guarantees marketing compliance of your promotional material.
Correctly set, confirmed prices are the key to product profitability and business success. Ensure the fastest way to market and controlled market access throughout the Nordic region.
Easy and efficient access to pharmacovigilance services: drug safety monitoring, reporting and management of safety risks.
Do you need an expert report or a training course? How are you at interpreting medical material? Our pharmacology specialists are here to help you.
Deepen your knowledge with the help of top-level experts. We have experience, expertise and insights to share.
Borderline products are subject to regulatory requirements and supervision to an increasing decree. Our competent Borderline team is here to help you.
Are you worried about multiple medications or continued use of drugs which may no longer be necessary? Do you suspect adverse reactions or interactions?
Do you need a locum, additional resources, special expertise or someone to manage a project? We will provide you with a flexible solution tailored to the changing needs of your company.
Our team will find fast and the most suitable routes for your company in different phases of the life cycle of your medical devices (MD or IVD devices).