Every testing project is reviewed by Quality Assurance for cGMP compliance.
Every aspect of our operations is monitored by QA through regular internal audits, training and document review.
MML has been providing Training for over 15 yrs to large Pharm-Med-BioTech companies in areas of :
- Test Methods, Protocols, Method Transfers
- Compendial protocols such as USP/EP/JP/ASTM/ISO methods
- Instrument startup and operation
- Instrument Performance Qualification or Maintenance
- Instrument Calibration
Documentation is the essence and fabric of Quality and Compliance in the GMP environment. MML utilizes SOP’s, Guidelines, Protocols, Worksheets, Forms and host of documented methods in every aspect of our operations
QA & Customer Service
Test methods are determined immediately upon receipt of samples or when we receive advanced notice.
Procedures for testing fit the scope of work and complexity, are customer approved and document all aspects of testing.
Testing Guidelines – simple one page description of small details, usually with reference to SOP’s.
Test Protocols – for more complex sample preparation such as medical devices or certain formulations.
SOP’s – the foundation of our document control process.
While Lab Notebooks are fully utilized, our customer document system provides simple, yet effective cGMP assurance that your sample preparation, testing and reporting are consistent.
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