Tablet Characterization with Regulatory Compliance Methods – USP<1062>

At Natoli Scientific, we’re in the lab every day compiling thorough USP <1062> Tablet Compression Characterization data to help you identify and solve compaction problems and provide solutions. If you’re still looking for the technology and information needed to satisfy industry regulations, look no further! In our new course, we’ll use regulatory compliance training to demonstrate the best practices to address solutions to the root causes of compaction issues like picking, sticking, low hardness and more!

Through a mixture of classroom and lab work, we’ll cover all of the elements required for particle characterization, effective formulation development, and tablet manufacturing.

You won’t get this level of quality instruction anywhere else. Sign up TODAY!

LEARNING OBJECTIVES:

• Role of material’s molecular and macroscopic properties on final attributes of compact/tablet
• Explain Tableting Profiles derived through Compactibility, Compressibility and Tabletability, speed sensitivity, and force-displacement to ensure USP <1062> Compliance
• Dynamic compression profile parametrization (Heckel analysis, SRS index, Work Descriptors) obtained with material sparing approach
• Quality Control of Pharmaceutical Materials using Material Sparing Approach
• Apply knowledge learned to use data acquisition hardware and software to collect and access detailed compaction analysis data

THIS COURSE IS DESIGNED FOR:

This course will benefit operators/technicians involved in the formulation, manufacturing and quality control process of tablets:

• R & D pre-formulation and formulation scientist
• Pharmaceutical Manufacturing Research & Development Staff
• QA/QC Analyst Technical /Quality Personnel
• Manufacturing & Process Development Operators, Engineers, Formulators
• Contract Manufacturing & Research Organizations
• Technical Services, Line operators and QA Specialist