No guide will replace the need to conduct process development and optimization experiments.
The unique nature of every process stream combined with application and regulatory requirements play a part in
determining the optimum process solutions. Use this selection guide as a starting point for selecting and sizing
the most appropriate Merck solutions.
We provide information and advice to our customers on application technologies and regulatory matters to the best of our knowledge and ability, but without obligation or liability. Existing laws and regulations are to be observed in all cases by our customers. This also applies in respect to any rights of third parties. Our information and advice do not relieve our customers of their own responsibility for checking the suitability of our products for the envisaged purpose.
The holder of the manufacturing authorization shall ensure that the excipients are suitable for use in medicinal products by ascertaining the appropriate good manufacturing practice. This is particularly true if the material in a certain application is regarded as high risk excipient, for example in parenteral dosage forms.