Granzer Pharmaceutical Services GmbH is committed to provide safe and efficacious medicinal products to the EU/EEA common market. To reach this goal, Quality is our core value.
All our employees understand and follow our standards and procedures in order to ensure product quality and regulatory compliance, and to protect the patient’s health and safety as our highest priority. We are all responsible for quality through our day-to-day activities.
Our quality culture drives continuous improvement and supports innovation. We are committed to pursuing an open dialogue with our employees, our clients and regulatory bodies. Our objective is to increase mutual understanding and to reinforce confidence in the way we conduct our activities.
To enable the availability of medicinal products with complex and diverse supply chains for the EU common market, we will guide our clients to develop products and establish supply chains that fulfill the high European standards. Therefore, we offer the following services:
Audits
Our experts will support your successful supplier qualification program. We conduct worldwide GMP Audits for the full spectrum of CDMOs.
QP Services
Our EU Qualified Persons provide Batch Certification and Release of IMPs for use in clinical trials in the EU.
Import / Storage
We act as Importer of your IMP or API into the EU from third countries (e. g. the USA or the People’s Republic of China). Imported material can be stored either at our facility or at qualified external partners in a GMP environment.
Consulting
We provide consulting for all GxP related areas. Together with our parent company, Granzer Regulatory Consulting & Services, we offer the full spectrum of pharmaceutical development consulting.
Reach out to our expert team to discuss how we can support you: