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Certificate

Pharmaceutical solid dosage forumulation

Candidates with sound knowledge of Pharmaceutical Solid Dosage Formulation are in high demand in the cannabis and pharmaceutical industry.

This training program on Pharmaceutical Solid Dosage Formulation examines current solid dosage technology and provides case studies for troubleshooting and investigational events for process deviations discusses QMS and GMP inspection preparation and provides process improvements and recommendations. Aspirants who want to become Formulation Technologists / Specialists, Formulation technicians, Up-stream technologists, Down-stream technologists, or Validation Specialists should attend the solid dosage formulation program.

Program code:

Credential:

Certificate

Duration:

Delivery Mode:

Online / Onsite / Recorded Program

Start Date(s):

January | May | September
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Program Overview – Pharmaceutical Solid Dosage Formulation

Professionals with expertise in Pharmaceutical Solid Dosage Formulation are in high demand across the cannabis and pharmaceutical industries. This specialized training program provides an in-depth understanding of solid dosage technology and its applications in modern pharmaceutical and cannabis manufacturing environments.

Program Offers

  • Register for 3 certificate programs at NACPT and get any available 1-day training for free.
  • Attendees will be issued the certificate of completion at the end of training program.

Learning Outcomes

After successful completion of this course, students will be:

  • Able to identify ideal drug
  • Able to formulate solid, liquid, and powder formulation
  • Able to check drug effectiveness
  • Able to scale-up production
  • Able to perform technology transfers

Program Module

  • Understand the solid dosage formation
  • Pharmaceutical regulatory requirements
  • Raw material Dispensing/Formulation, Blending
  • Direct Compression
  • Wet Granulation
  • Dry Granulation

  • Drying, Compression/Encapsulation
  • Coating, Packaging and Receiving/Warehousing Operations
  • Manufacturing equipment and the technology advancements for drug optimization
  • An overview of product characteristics and how they dictate the unit operations method

  • Effective process monitoring techniques during the scale-up and technology transfer processes
  • A summary of the principles of QBD in OSD manufacturing processes

  • GMPs influence unit operations and subsequent equipment design, production suite design, control and monitoring requirements
  • An analysis of PAT, PPP, MES, CMP, and PLC