With the rapid pace of innovation in the MedTech market, projected to reach a volume of $772.5 billion by 2029, teams need a streamlined approach to product development, ensuring that safety, compliance, and efficiency are prioritized throughout the medical device lifecycle.
Why it matters: Overcoming siloed work between key functions and phases of the Total Product Lifecycle (TPLC) for medical devices is essential for improving medical device outcomes. When these functions and phases operate in isolation, it can lead to delays, compliance issues, and inefficiencies, all of which hinder a product’s success.
The solution: An integrated workflow framework, applied throughout the TPLC offers a powerful solution to break down silos, create efficient workflows, and align key functions and phases. By fostering collaboration through a shared framework, these combined workflows ensure that compliance, development, and engineering are synchronized with continuous feedback, improving product quality and safety, and speeding up time to market.
What you’ll learn in the white paper:
- The functions and phases of the Total Product Lifecycle (TPLC) for medical devices.
- Challenges faced by project teams in each phase and function of the TPLC.
- What an integrated workflow framework is and how to apply it to medical device development.
- Strategies to streamline workflows, ensure compliance, and accelerate time to market.
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Complete the form below to download your copy of the white paper and discover how to navigate the complexities of MedTech device development.
Contributing experts: Stefan Mrsic, Nemanja Kovacev, Milos Cigoj, Adana Micu, and Dejan Igumanovic
