Granzer Regulatory Consulting & Services was founded at the beginning of 2002 by
Dr. Ulrich Granzer and offers a wide range of services in the field of regulatory affairs.
Our team comprises a staff of experienced consultants who have backgrounds in large and small pharma as well as biotech. They have know-how and proficiency in the various disciplines required for drug development.
No matter, if you are an SME or a large pharma company, we support you in 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.
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 authority meetings, 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.
Our success is measured by our customers’ satisfaction.