Pharmaceutical testing
Method development and validation
Method development
and validation, to ICH guidelines, is undertaken. An experienced
member of staff will discuss your requirements with you and
assist in the design of the study plan.
Once this is agreed,
our laboratory staff provides the accurate data to support
the method viability.
On completion of this stage (and following
appropriate QA inspection), a draft report is prepared and
submitted to the client for approval. Examples include:
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Confirmation
of stability under stipulated conditions |
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Indication
of extent of loss of active principles under adverse
storage conditions |
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Development and validation
of batch release methods |
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