training heading content

Natoli Scientific Training: Tablet Characterization with Regulatory Compliance - USP <1062>

Understand the best practices to address issues of tablet compaction by securing the USP <1062> data you need to ensure you’re in full compliance. Let us teach you practices for identifying your compaction problem – picking, sticking, binding, capping, low hardness – this training examines root causes and provides solutions.

Complete the form below to register for this training course.

Date: February 16–18, 2027
Location: Natoli Scientific, Telford PA

Prices:

  • $2,995/person
  • $2,695/person (individual before February 5, 2027)
  • $2,425/person (groups of two or more before February 5, 2027)

Learning Objectives​

  • 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

  • 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

Register Now

Seating is limited. Take advantage of our group and early registration discounts.