Tablet Characterization with Regulatory Compliance – USP <1062> (Sept 9-11)
Date: September 9-11, 2025
Location: Natoli Scientific, Telford PA
Cost: $2995
Early Bird Special: $2695
Seating is limited. Ask about our group discounts.
Download BrochureLearning Objectives
Participants of this training course will finish with an understanding of these concepts:
- Role of Material’s Molecular and Macroscopic Properties on Final Attributes of Tablets
- Dynamic Compression Profile Parametrization (Heckel analysis, SRS index, Work Descriptors)
- Explain the Components and Operations of Formulation Selection
- Data Acquisition Hardware & Software to Collect Detailed Compaction Analysis Data
- Independently Perform Tableting Operation & Manufacturing Equipment Setup
- Quality Control of Pharmaceutical Materials
- Identify and Resolve Common Manufacturing Equipment Challenges
- Tableting Profiles Derived Through Compactibility, Compressibility and Tabletability, Speed Sensitivity, and Force-Displacement to Ensure USP <1062> Compliance
Who Should Attend?
This course was designed to benefit industry professionals in the roles of:
- 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
- Maintenance Technicians
- Supervisors & Production Support
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