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For more than 30 years, PharmAssist has a proven track record of successful engagement in custom method development and validation for a range of pharmaceutical products at different stages of development with emphasis on chromatographic techniques. Our highly trained staff works in a practical, GMP-compliant manner to achieve sound methods that will uphold successful DP filings and be dependable and robust in the future.

A comprehensive method development and validation report is sent to our clients upon completion of the studies. PharmAssist helps clients transfer the method to their own laboratory, through written protocols and telephone conversations with the appropriate personnel, and/or by on-site visits to the client's laboratory. PharmAssist can also serve as an outside laboratory to critically evaluate new methods developed by the client, prior to their implementation. This valuable service provides additional ruggedness data and helps to unmask potential problems with the method before problems occur in the QC lab.

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