Granzer Regulatory Consulting & Services offers a wide range of services in the field of regulatory affairs. Our support covers all phases of drug and device development, from defining the right development strategy to submitting your marketing authorisation application, as well as the regulatory maintenance of your products.
No matter, if you are an SME or a large pharma company, we support you right from the start of the development and regulatory process. We assist you in the development of the best road map and the definition of the right time for the first contact with relevant regulatory authorities. We facilitate , help you prepare the necessary briefing packages containing a full development strategy and accompany you in all phases of interactions with regulators including dossier preparation and full regulatory submissions.
Further value to your business can be offered in co-operation with our partner organisation, which provides strategic and operational consultancy services in business development, licensing and company strategy.