Validation Solutions
Ensure consumer safety with validation, qualification, and calibration solutions from Ellab. Buy or rent our industry leading wireless data loggers, thermocouple systems, and our time-saving FDA compliant software for your critical processes.
Monitoring Solutions
Maintain the integrity of your valuable products by reliably monitoring their environment. Get a single overview of all your applications and be notified as soon as conditions fall outside your predefined parameters.
Field Services & Consulting
With local teams around the world, we stand ready to consult, qualify, validate, and calibrate your critical GMP processes more efficiently than any other supplier with our industry-leading validation solutions and consulting expertise.
Why do business with Ellab?
Industry leading solutions & services
FDA 21 CFR part 11 compliant
Decades of validation & monitoring expertise
Leading software with the most reliable data integrity
High quality & accurate hardware
Fast and efficient service & support
Innovative engineering
Local partnerships & support
8 Reasons Ellab Continues to Inspire Trust
With the satisfaction and well-being of our customers as our highest priority, we continue to provide top quality services and products in the best ways possible. Our dedication and growth can be traced through various figures across all fields.
9.000
+
Active systems worldwide
80
+
Offices and distributors worldwide, of which 20+ have calibration facilities
100
%
Renewable Electric Energy and commitment to near-term SBTi targets
800
+
Great employees, of which 370+ are field service engineers
93
%
Of customers would recommend or strongly recommend Ellab to others
89
%
Of employees are satisfied or very satisfied with working at Ellab
73
/100
Top global biotech and pharma companies use Ellab
82.000
+
Calibrations performed annually
Gain Valuable Insight with our Blog
On the Ellab blog we share all our knowledge and rare insight so we can work together to ensure consumer safety.
Visit the Ellab Blog18 September 24
Common Compliance Issues in GxP Audits and How to Address Them
In the pharmaceutical and biopharmaceutical industries, staying audit-ready is vital for regulatory compliance: common compliance issues often occur during GLP and GMP audits, making a solid understanding of GxP requirements key to preventing operational setbacks.
Read more26 August 24
What You Need to Know About Environmental Monitoring in Life Sciences
Environmental monitoring in life sciences is essential for ensuring product safety, regulatory compliance, and overall operational integrity.
Read more08 August 24
How to Qualify an Incubator: A Comprehensive Guide
Discover how to qualify an incubator with our comprehensive guide; ensure compliance, sample integrity, and optimal laboratory conditions.
Read more18 July 24
Ensuring Quality: How Equipment Validation Supports GMP Compliance
Equipment validation and Good Manufacturing Practices (GMP) are interlinked in ensuring the production of high-quality, safe products.
Read more11 July 24
What is Calibration? Understanding the Basics and Importance.
In simple terms, calibration means comparing the accuracy of an instrument, such as a thermometer, with a known accurate reference device, known as a calibrator.
Read more26 June 24
Test your Data Integrity with These 12 Questions
Maintaining the integrity of your data is essential when performing continuous monitoring of rooms, chambers, and storage, especially in the life sciences industry.
Read more11 June 24
Overcome Your Incubator Challenges with Continuous CO2 Monitoring
Continuous monitoring is crucial in the biotech and pharmaceutical industries, where precise control of environmental conditions ensures product quality, safety and regulatory compliance.
Read more30 April 24
Preparing for the Heat: Summer Temperature Mapping Studies for Pharmaceutical Integrity
The integrity of temperature-sensitive products are at stake during the hot summer months.
Read more19 April 24
What You Need to Know about a Risk-Based CSV Approach
In the biopharmaceutical field, it's essential for regulatory, clinical, and IT staff to make sure computer systems work well by using smart computer system validation methods (CSV).
Read moreNeed to stay compliant and keep your biopharmaceutical products safe?
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