Celegence provides services and solutions to support the Life Sciences industry with regulatory affairs operations and strategy. We aim to help Life Sciences companies navigate complex global regulatory requirements by providing depth of experience and an extensive delivery capability.

As regulatory specialists, we work across all phases of the product lifecycle from regulatory strategy, authoring, and all aspects of established product maintenance, including submission management, publishing and health authority interaction. We leverage a global team of consultants to provide local regulatory insight, strategy and intelligence.

Our mission is to collaborate with our customers to deliver Regulatory Affairs efficiency that allows them to focus on what matters most: providing exceptional patient value. We support companies in ensuring regulatory compliance across the globe by providing fully trained resources who understand the regulations and can leverage this knowledge to assist our clients in their day-to-day operations.

Celegence is a privately owned business headquartered in Chicago, IL with offices in the U.K., Europe, and Bangalore(India).



Life Sciences

Celegence

Celegence's headquarters in Downers Grove, IL, United States

Punya Abbhi

Lakshmeenarayana G Goundalkar

Matt Tyler

Erin Cosgrove

Mukesh Chandra Pandey

Adarsha Sheshagiri Mavinakulli

The Medical Device Specialists team at Celegence focuses on navigating the complex regulatory landscape for medical devices throughout the product lifecycle. This team collaborates with clients to develop and implement regulatory strategies, manage submissions, and ensure ongoing compliance with global regulations. With a blend of expertise in regulatory affairs, quality assurance, and medical writing, they empower Life Sciences companies to streamline their operations and enhance patient value effectively.

Medical Device Specialists

The Regulatory Affairs and Compliance team at Celegence specializes in guiding Life Sciences companies through the complexities of global regulatory frameworks. By developing regulatory strategies, managing submissions, and ensuring compliance throughout the product lifecycle, the team enhances operational efficiency. With a diverse group of experts, they provide local insights and foster collaboration, enabling clients to focus on delivering exceptional patient value.

Regulatory Affairs and Compliance

The Leadership Team at Celegence is responsible for steering the company's strategic direction and operational efficiency in the Life Sciences regulatory landscape. Comprising key executives such as the Chief Delivery Officer and Chief Scientific Officer, this team focuses on enhancing service delivery, fostering business development and partnerships, and ensuring alignment with industry standards. They collaborate to optimize regulatory strategies, drive growth, and maintain a commitment to exceptional client service and patient value.

Leadership Team

The Engineering and Technical Roles team at Celegence is responsible for developing and maintaining innovative software solutions that enhance regulatory affairs operations within the Life Sciences industry. This team collaborates closely with regulatory specialists to create tools that facilitate compliance, streamline submission processes, and improve overall operational efficiency. With a focus on technical excellence and user experience, the team ensures that clients can navigate complex regulatory requirements effectively while enabling seamless integration of technology in their workflows.

Celegence

Org chart

Teams

Medical Device Specialists

Regulatory Affairs and Compliance

Leadership Team

Engineering and Technical Roles

Offices

Celegence

Org chart

Teams

Medical Device Specialists

Regulatory Affairs and Compliance

Leadership Team

Engineering and Technical Roles

Offices

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