Quality Assurance and Quality Control for Biotech Industries
Discover essential strategies for optimizing quality assurance and control in biotech industries. Ensure FDA compliance and improve product safety today. Quality Assurance and Quality Control Did you know that the global biotech industry is expected to be worth more than $3 trillion by 2030? With a number like that, it isn’t surprising that biotechnology is gathering […]
CDISC SEND Controlled Terminology Best Practices
Blog Are “Not Done” and “NOT DONE” the same? Not in CDISC SEND controlled terminology. The correct use of controlled terminology is a critical part of submitting study data to the FDA. It can be challenging, though. A PDF of the current CDISC SEND controlled terminology has several pages. It includes thousands of terms and […]
Best Practices for Enabling FDA SEND Compliance
Blog What is FDA SEND Compliance? The Clinical Data Interchange Standards Consortium (CDISC) created the standard. FDA SEND supports the approval process. SEND stands for the Standard for Exchange of Non-clinical Data. It’s vital to follow FDA SEND compliance regulation guidelines to streamline the approval process. The Study Data Tabulation Model(SDTM)is a standard for organizing […]
A Guide on FDA Study Data Submission Requirements
A Guide on FDA Study Data Submission Requirements The Challenges in Complying with SEND The evolving guidance of the FDA on nonclinical dataset submissions requires organizations to adapt procedures to ensure full regulatory compliance. The Food and Drug Administration rejects as many as one in three study data submissions due to technical factors. Nonclinical studies […]