We are visiting IFPAC. See you at Booth 211 from March 3 - March 6, 2024 Learn More

Connect CPV™ is a cutting-edge digital SAAS solution that ensures real-time monitoring, compliance, and optimization of pharmaceutical processes for enhanced product quality and regulatory confidence.

Mareana
Connect
CPV™

Digital Twin
Native

Create end-to-end batch genealogy with forward and backward data traceability and easy visual navigation across all process steps for root cause analysis.

Improved Yield &
Capital Efficiency

Extract vital insights for process enhancement, release on-hold batches through data-driven decisions to improve yield and unlock capital from built-up inventory.

Streamlined
Compliance

Provide automated reports for compliance filing and leverage all data sources to minimize errors.

Automated Data
Processing

Extract & contextualize data from paper-based & third-party sources with automated data validation framework.

AI-Driven
Excellence

Enable real-time release & continuous quality control for optimal efficiency.

Integrated Enterprise
Solution

Deliver real-time insights to enhance efficiency across the entire drug manufacturing process with contextualized data. Integrated Data Science Studio equipped with multivariate analysis capabilities, and comprehensive statistical process control charts, eliminates the need for multiple systems.

Mareana Connect CPV™ - A Step Ahead

Improve Predictability

Ensure consistent product quality in every batch while optimizing yield

Amplify Productivity

Streamline manual processes and ease operations using a single source-of-truth

Simplify Compliance

Automatically generate compliance reports and standardize procedures

Reduce Expenses

Conserve resources through automation and minimize waste

Answer: By providing real-time insights and analytics, our solution enables proactive decision-making, minimizes downtime, optimizes resource utilization, and enhances overall efficiency throughout the manufacturing lifecycle.

Answer: Connect CPV™ is designed to align with industry regulations, offering features like automated documentation, audit trails, and real-time reporting to support compliance with regulatory standards.

Answer: Yes, our solution is designed to seamlessly integrate with various manufacturing systems and databases, facilitating a unified and efficient data flow across the production environment.

Answer: It is equipped with advanced analytics and anomaly detection algorithms. When deviations occur, the solution triggers alerts, enabling proactive intervention to address issues promptly and maintain product quality.

Answer: The solution employs robust security protocols, including encryption, access controls, and audit trails, to ensure the confidentiality, integrity, and availability of sensitive manufacturing data.

Answer: Yes, our solution is designed for scalability, allowing seamless deployment and adaptation to various production environments and facilities, whether local or global.

Answer: It provides a centralized platform for stakeholders to access real-time data, collaborate on quality issues, and streamline communication, fostering a more integrated and responsive manufacturing ecosystem.

Connect With Our Team

"*" indicates required fields

Blogs

female hand holds a magnifying glass over pills

Demystifying Regulatory Compliance

AI or Artificial intelligence is being used to develop new drugs

AI in Accelerating Drug Development and Production

Doctor fills out the medical survey paperwork

Continued Process Verification Guidelines