Midwest Compliance Laboratories
Midwest Compliance Laboratories, LLC is a quality control laboratory founded in 2008, specializing in contract analytical testing services for pharmaceutical and related industries. They focus on providing reliable, compliant, and cost-effective testing with a commitment to customer needs, fast turnaround times, and high standards of quality and integrity. The company is FDA registered, DEA licensed, ISO 9001:2015 registered, and GMP compliant, with a team of highly trained scientists dedicated to excellence in laboratory testing.
Industries
Nr. of Employees
small (1-50)
Midwest Compliance Laboratories
Terre Haute, Indiana, United States
Products
Stability Storage
Ample storage capacity utilizing three large walk-in chambers and several reach-in chambers controlled to any ICH storage condition for stability studies.
Method Development and Validation Services
Custom analytical method development, method transfers, and method validation provided by senior scientists for your analytical projects.
Microbiology Testing Services
Top-tier microbiology testing services dedicated to ensuring the highest quality and safety standards for pharmaceutical products.
Stability Storage
Ample storage capacity utilizing three large walk-in chambers and several reach-in chambers controlled to any ICH storage condition for stability studies.
Method Development and Validation Services
Custom analytical method development, method transfers, and method validation provided by senior scientists for your analytical projects.
Microbiology Testing Services
Top-tier microbiology testing services dedicated to ensuring the highest quality and safety standards for pharmaceutical products.
Services
Instrumental testing services for pharmaceutical products using chromatography, mass spectrometry, spectroscopy, and titration methods.
Testing of tablets and capsules for dissolution, disintegration, and hardness.
Analytical testing of raw materials used in manufacturing.
Storage and management of stability study samples in chambers controlled to ICH conditions with on-site capacity.
Analytical method development for new products, method transfer services, and formal method validation performed by senior technical staff.
Standardized sample submission process with chain-of-custody documentation for tracking submitted samples.
Instrumental testing services for pharmaceutical products using chromatography, mass spectrometry, spectroscopy, and titration methods.
Testing of tablets and capsules for dissolution, disintegration, and hardness.
Analytical testing of raw materials used in manufacturing.
Storage and management of stability study samples in chambers controlled to ICH conditions with on-site capacity.
Analytical method development for new products, method transfer services, and formal method validation performed by senior technical staff.
Standardized sample submission process with chain-of-custody documentation for tracking submitted samples.
Expertise Areas
- Quality control laboratory testing (pharmaceuticals)
- Analytical chemistry and instrumental analysis
- Stability study storage and management
- Analytical method development and validation
Key Technologies
- High-performance liquid chromatography (HPLC)
- Gas chromatography (GC)
- Liquid chromatography–mass spectrometry (LC-MS)
- Atomic absorption spectroscopy (AA)