Regulatory Services
Regulatory Services
GRC provides expert regulatory consulting services, guaranteeing compliance with both national and international regulatory requirements. Our team offers comprehensive support for navigating the intricate regulatory landscape of clinical trials, ensuring efficient approval processes and adherence to all legal and ethical standards. Our Regulatory Services include:
Consulting on National/International Regulatory Requirements:
Regulatory Liaison for Clinical Trial Permission:
Safety Reporting:
Import License for Investigational Medicinal Products (IMP):
Export License for Biological Samples:
Common Technical Dossiers (CTD, eCTD) Preparation:
With GRC‘s regulatory services, clients can be assured that their clinical trials will comply with all regulatory requirements, facilitating successful trial progression and product approval.
