Manage change and drive innovation. Equip your business with the technologies, partners, and expert guidance to navigate uncertainty and thrive.
New regulations, technological advancements, mergers and acquisitions: Change is constant in the medical device industry, and it can cost a lot of time and resources.
Switching devices or processes typically involves modifications across various types of records — design control records; device master records (DMRs); production, validation, and regulatory documents. Document-review meetings are time-consuming, involving cross-functional team members from multiple international facilities and business divisions.
Wipro mitigates these challenges by connecting manufacturers with a vast network of experts and services to help them keep pace with change. Our teams review documents, evaluate systems and processes, to ensure clients are up to date, compliant, and as efficient as possible. With continuous support and guidance, we shall help your business navigate the changes common in the industry today.
- QMS implementation
- Regulatory transitions
- Product lifecycle maintenance
- Platform change/implementation
- Supplier change management
- Implementing GxP systems by effective change management