Industry Progress Towards Unified Operations
As the global regulatory landscape continues to evolve, many medtech organizations are transforming systems and processes to ensure compliance.
The Veeva MedTech 2021 Regulatory Benchmark Report examines the medical device and diagnostic industry’s progress towards modernizing regulatory operations by gathering the experiences of regulatory affairs professionals from nearly 100 global organizations.
The study results show that while there are positive signs of moving toward unified regulatory processes across divisions and geographies; manual methods, data governance, and siloed systems are still present in many organizations.
- 67% have identified areas where digital technology is needed
- 62% have selected digital technology
- 56% already have harmonized global processes across regulatory affairs
Download the full report to gain insight into the current state of regulatory affairs modernization across areas including global compliance and visibility, speed to market, and postmarket surveillance. The report also includes best practice recommendations.