QC is a process to ensure quality, accuracy, and consistency of clinical documents, and that standards of regulatory authorities and contracted services are met.
Elements of QC
- Data verification: 100% verification of data and confirmation of non-numerical data
through source document review - Consistency and organization: Adherence to style guidelines and precise messaging
- Source verification: Ensuring accuracy and validity of all cited sources to reduce misinformation
- Formatting and structure:Use of correct formatting, structure, and approved templates
Key Attributes of Quality Control Specialists
- Deliver high-quality documents through precision, compliance, and clarity
- Diverse skill set and highly trained
- Fresh perspective. A fresh pair of eyes not involved in the writing to guarantee accuracy and consistency
- Understand and adapt to changes in timelines or regulatory agency modifications
Benefits of Partnering with Syner-G for QC
- Our experts have built trust and credibility within the pharmaceutical industry and regulatory agencies.
- Experts at early detection of errors post-writing process.
- We provide a comprehensive review of documents.
- Your project has a dedicated and committed QC team to ensure high standards.
