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Post-Mergers & Acquisitions (M&A) Integration

Harmonise | Comply | Sustain

Post-Mergers & Acquisitions (M&A) Integration

Post-Mergers & Acquisitions (M&A) Integration

Harmonise | Comply | Sustain

Enabling Seamless Mergers and Acquisitions through Compliance-Driven Services 

In the dynamic landscape of MedTech M&As, the need for seamless integration has intensified. From cross-border deals to acquiring digital health innovations, embracing vertical integration, and consolidating in niche markets, many factors drive M&A in the medical device industry.

The challenges such as integration complexities, regulatory hurdles, financial risks, and soaring integration costs, highlight the importance of adept Quality Assurance and Regulatory Affairs (QARA).

Tata Elxsi is your strategic partner in navigating the complexities of MedTech M&A integration. Our solutions include post-acquisition due diligence, facilitating a seamless transition, QARA solutions like QMS integration, DHF creation and remediation, risk management. We also provide support for labeling, IFU, drawing, and packaging. With expertise in manufacturing documents, biocompatibility, clinical compliance, and regulatory submissions, Tata Elxsi ensures a seamless integration process that provides a resilient foundation for MedTech companies to thrive.

Here's how we can help you

Here's how we can help you

Here's how we can help you


Comprehensive regulatory due diligence for acquired product portfolios

  • Assess compliance history to identify regulatory risks and liabilities

Integration of products and quality processes for compliance

  • Proactively address evolving compliance requirements to mitigate risks

Streamline operational efficiencies post-acquisition

  • Implement product and quality change management processes for sustained compliance
  • Optimise product portfolio documentation by creating product families and groups

Service Framework

Post-Mergers & Acquisitions (M&A) Integration

Why Tata Elxsi?

  • Collaborate with integration planning teams during the due diligence phase to define objectives and achieve the plan goals

  • Catalogue pricing and an outcome-based commercial model to support customers through the unpredictable variability and volume of activities

  • Compliance assurance model with a track record of transformative productivity gains

  • Certified engineers, regulatory and quality experts along with comprehensive in-house training modules to ensure fast ramp-up

  • Data security in compliance with ISO 27001:2013, ISO 13485 QMS certification, 21 CFR Part 820

Automating Regulatory Intelligence for the $10 Trillion Global Healthcare Market
Business Whitepaper

Automating Regulatory Intelligence for the $10 Trillion Global Healthcare Market

Ensuring Uninterrupted Sales Of Legacy IVD Devices in the EU Market
Case Study

Ensuring Uninterrupted Sales Of Legacy IVD Devices in the EU Market

Driving QARA Programs through a Global Engineering Network
Case Study

Driving QARA Programs through a Global Engineering Network

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