General description
Pharmaceutical secondary standards for application in
quality control provide pharma laboratories and manufacturers with a convenient
and cost-effective alternative to the preparation of in-house working standards
Application
These Secondary Standards are qualified as Certified
Reference Materials. These are suitable for use in several analytical
applications including but not limited to pharma release testing, pharma method
development for qualitative and quantitative analyses, food and beverage
quality control testing, and other calibration requirements.
Analysis Note
These secondary standards offer multi-traceability to the
USP and EP primary standards, where they are available.
Other Notes
This Certified Reference Material (CRM) is produced and
certified in accordance with ISO 17034 and ISO/IEC 17025. All information
regarding the use of this CRM can be found on the certificate of analysis.
To see an example of a Certificate of Analysis for this
material enter LRAA6959(changes by product) in the Documents slot below. This
is an example certificate only and may not be the lot that you receive.
