The scope of ICRC-WEYER services spans the entirety from preclinical to phase I-IV, health claim and post-marketing studies for pharmaceutical, biotech and nutrition companies.

ICRC-WEYER has a long history of delivering the high quality clinical trials required for the pharmaceutical development process within its complex regulatory framework.

With the arising regulatory hurdles in the nutritional business sector and the evolving need for scientific substantiation of health claims, ICRC-WEYER has also developed extensive experience in the conduct of clinical trials on the background of the requirements of the European Food Safety Authority (EFSA).

We offer an all-round package comprising scientific consulting on the optimal trial design, highly professional trial conduct, integrated data management and data analysis as well as integrated medical writing services.

ICRC-WEYER offers its services either separately or as synergistic multi-service packages.

ICRC-WEYER enjoys close partnerships with other service providers and independent experts and can look back on 20 years of experience working with partners and clients ranging from university researchers to major food ingredient producers and global pharmaceutical companies.

Our services include:

• Biostatistics
• Data Management
• Independent Expert Medical Review
• Medical Writing
• Clinical Monitoring
• Pharmacovigilance
• Regulatory Services
• Scientific Consulting
• Study conduct