The Preferred Solution for Contract Labs

Reliably meet SOPs, build trust through reporting, and fuel your growing operations.

Helping you Grow with Confidence

Born in a contract research organization, CellPort helps you achieve better outcomes for your cell-based operations.

Regenerative
Medicine

Stem Cell
Technology

Cell & Gene Therapy (CGT)

Cellular Agriculture

How CellPort Supports CROs and CDMOs

CellPort empowers contract labs to achieve better outcomes with streamlined upstream (USP) and downstream (DSP) processes, such as:

Cell Line Identification & Tracing

Cell Culture, Banking, & Storage

Master Batch Records (MBRs)

Customized Reporting

SOP Adherence

Yield & Viability Optimization

Regulatory Compliance

Media Preparation

Quality Control

Finish & Fill

Why Scientists Love CellPort

Watch this guided walkthrough to learn how CellPort streamlines cellular processes for contract research, development, and manufacturing labs.

SOP Adherence

With the enormous scale and complexity of most cell-based operations, CROs and CDMOs risk falling behind due to changing schedules and overwhelming task lists – especially when using paper or simple spreadsheets to conduct project management. Moreover, new technicians require ample time to learn new processes, leading to potential mistakes with downstream impacts.

To ensure reliable, reproducible results within deadlines, project managers must have oversight of thousands of activities that occur throughout the R&D and manufacturing processes. Once delegated to the proper person, managers must track completion and ensure all tasks are completed on time using the appropriate standard operating procedures (SOPs).

With smart lab management solutions like CellPort, managers can ensure high-priority tasks are handled at the right time, with easily generated calendar views that notify teams of upcoming tasks, missed tasks, nearing expirations, and completion of preconditions. CellPort’s digital protocols act as a central repository for rapid upskilling, with real-time tracking to ensure SOPs have been followed.

Handle Audit Requests Faster

Identify and deliver findings with verified meta-data, e-signatures, and all compliance requirements included.

Explore Regulatory Compliance Features

Customized Reporting

Give clients and leadership real-time insights into the progress of cell-based operations with centralized stores of validated data.

With CellPort, you can generate cell lineage mapping, resource optimization to save costs, productivity assessments, AI-powered projections (coming soon), and many more client-facing reports.

Learn more about CellPort’s Customized Reporting tools today.

Explore Customized Reporting

Spark Collaboration Like Never Before

Store observations, notes, approvals, and documents on an easily searchable communications & data analytics hub – With CellPort, you can assign tasks, see the status of activities, auto-schedule future events, and safely share relevant information with the right people.

Explore Collaboration Features

Stay Secure on Industry-Leading Cloud Provider

Built on the cloud platform trusted by 95% of Fortune 500 companies, CellPort is designed from the ground up to keep your client’s valuable data & IP safe.

CellPort has been ISO 27K certified.

Explore Secure Cloud

CellPort Features

Built by our scientists, for your scientists – Here’s how CellPort helps optimize cell culture and passaging.

Digital Protocols

Choose from a library of pre-built or custom digital workflows and assays.

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Master Batch Records

Streamline cell manufacturing in a safe and compliant lab environment.

Coming Soon

Resource Tracking

Optimize how you manage consumables, people, and more.

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Collaboration

Keep offline communication online for better transparency, traceability, and training.

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Customized Reporting

Monitor the status of your lab with real-time reporting and data analysis.

Coming Soon

Secure Cloud

CellPort is built on the cloud platform trusted by 95%of Fortune 500 companies, designed from the ground up to keep your data safe.

Explore More Industries

Biopharmaceutical

Facilitate more reproducible, GMP-complaint drug discovery & pharmaceutical manufacturing processes.

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Biotechnology

Optimize all upstream (USP) and downstream (DSP) operations with CellPort.

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Cellular Agriculture

Harvest a more plentiful cell culture with a reliable, consistent supply of cells.

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Academia, Teaching and Research

Train and upskill the next generation of scientists and lab technicians.

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CellPort Learning Hub

Browse our latest resources to learn more about how CellPort streamlines life sciences.

Products Videos

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Reporting

MBRs

Inventory

Protocols

Latest Blogs

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Research

3/12/25

CellPort: The Cell Culture Management Software

CellPort Software optimizes cell culture management, reducing errors and improving efficiency. Track media, schedule tasks, and access cell history in real-time with barcode scanning and custom reporting.

Manufacturing

3/4/25

CellPort Benefits

Discover how CellPort Software enhances operations by improving efficiency, data management, and compliance. Learn how our platform supports teams in optimizing workflows and driving success across all stages of development.

Research

2/26/25

Unlocking Insights from the Cell’s Journey Through Laboratory Operations: Metadata for Enhanced Understanding

Discover the importance of capturing metadata throughout the cell's journey in the lab, from materials to human observations. By tracking these interactions, researchers gain valuable insights, enhance reproducibility, and optimize workflows. CellPort enables seamless data capture, ensuring traceability, compliance, and efficiency across lab operations.

Development

12/4/24

Navigating the Regulatory Landscape in Cell-Based Operations

In the intricate world of cell-based R&D, Good Laboratory Practices (GLP), and Good Manufacturing Practices (GMP) laboratories, the stakes couldn't be higher—pioneering research and life-saving therapeutics stand as the pillar of achievements. Yet, the stakes are equally high in the realm of regulatory compliance. Stringent standards such as 21 CFR Part 11, Annex 11, ISO 27001, and GAMP 5, 2 ed. are not just demanding; they're the prerequisites for scientific veracity and patient safety.