Clinical Trial Regulations With ICH GCP E6 R2 Workshop

The Clinical Trial Regulations With ICH GCP E6 R2 Workshop covers topics such as:

• EU Annex 13
• GCP requirements for the sponsor related to IMP
• Distribution to sites
• Handling of IMP at sites
• Handling of IMP temperature deviations and complaints
• Transfer of IMP between sites

The Clinical Trial Regulations With ICH GCP E6 R2 Workshop brings together:

• Biotech companies
• Clinical Research Organizations
• Large to small Pharmaceutical companies
• Clinical Research Services Suppliers
• Non-Commercial Research Organizations