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About Us
Our History
Founded on May 6th, 1983, as Berdovich and Associates by Dan and Arlene Berdovich, our journey began as an applications consultant supporting pharma, biotech, and medical device manufacturers with formulation development.
With a deep understanding of various applications and technologies, Micro Measurement Laboratories, Inc. was established in 1998 to meet customer needs through individual sample testing. Today, we provide our services to pharmaceutical companies, biotech firms, and cutting-edge medical device manufacturers of all sizes worldwide.
Located in Wheeling, IL, we are a small, privately owned company operating out of a 10,000 square foot facility equipped with state-of-the-art facilities designed for sensitive particle work.
At MML, we are committed to delivering the highest quality products and cGMP test results promptly. Our primary objective is to ensure the utmost quality in all aspects of our operations while maintaining direct, open, and honest communication to transform data into valuable information for our customers.
Our Approach
Commitment to Quality and Customer Satisfaction
At MML, quality and customer satisfaction are our top priorities. We are dedicated to achieving the highest standards in every aspect of our operations, ensuring that our products and test results are delivered with unparalleled quality and efficiency.
Adherence to Industry Standards
We operate in strict compliance with current Good Manufacturing Practices (cGMP). Our goal is to consistently meet or exceed the specifications outlined in our Quality Program, ensuring that every product and test produced by MML upholds our commitment to excellence.
Our Approach to Excellence
To support our high standards, MML implements the following practices:
- Comprehensive Documentation: We maintain an extensive library of Standard Operating Procedures (SOPs), protocols and product specifications to ensure consistency and accuracy in our operations.
- Rigorous Testing Procedures: All tests are performed and documented according to established procedures and cGMP requirements, ensuring the highest level of data integrity.
- Continuous Training: Ongoing training for all our employees ensures that our employees maintain an in-depth knowledge of cGMP requirements, current compendial requirements (USP/EP/JP/BP/ASTM/ISO), and internal SOPs.
- Regular Audits: We conduct routine internal, customer, and FDA audits to ensure compliance and identify areas for improvement.
- FDA Registered Generic Drug Testing Facility
- ISO 17025 Accredited
