This webinar will show how a properly chosen, developed and validated method for assessing the solid state of the drug substance can be done efficiently in a phase-appropriate manner.

TORONTO (PRWEB)
February 18, 2021

Solid oral dosage drugs typically require knowledge and control of the solid form (e.g., polymorph, hydrate, solvate, co-crystal, amorphous) before the final formulation is developed. The physical form of the drug affects the properties and overall performance (e.g., solubility, bioavailability, stability and purity) for the drug product used by patients. In many cases, it is necessary to have a solid form specification for the drug substance throughout most of the manufacturing process. This webinar will show how a properly chosen, developed and validated method for assessing the solid state of the drug substance can be done efficiently in a phase-appropriate manner.

Join Dr. Patrick Tishmack, General Manager, AMRI in a live webinar on Tuesday, March 9, 2021 at 1pm EST to learn about choosing and developing methods for assessing the solid-state of oral drugs.

For more information, or to register for this event, visit Solid-State Method Development & Validation.

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