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  Training Agenda Lyophilization Basics for Pharmaceuticals: History, Scientific Principles, Cycles and Formulations
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An Overview of Lyophilization Pharmaceutical Course

This Lyophilization Pharmaceutical Course is sure to act as an outline for freeze-drying of pharmacological parenteral products. Many medicine substances necessitate the extra protection that lyophilization usually comes with, and the preparation of the liquid drug product must be designed to enhance the efficiency of the completely dried product. This course will cover multiple objectives right from how lyophilization functions to changing a liquid drug product into a dried, more-stable powder. Cycle and preparation design will be elucidated, along with the methodical values that are at play.

Reasons for You To Attend Lyophilization Pharmaceutical Course:

To study the process and reasons for formulating and designing lyophilization cycles for drugs that will gain an advantage from the freeze-drying procedure

Learning Objectives

▪         Definition of freeze-drying or Lyophilization

▪         Classify perfect features of a freeze-dried product

▪         Regulate when freeze-drying is essential

▪         Phases of the lyo cycle, and the methodical principles that drive each stage

▪         Framing drug products for fruitful freeze-drying

▪         Analytical tools used to aid in the formulation and cycle development


Section 1: History and background

▪         Definition of freeze-drying or Lyophilization, history, and commonly freeze-dried materials

▪         Anticipated freeze-dried features

▪         Rewards/ advantages and limitations of freeze-drying

▪         Procedure overview


Section 2: Physical, chemical, and engineering principles

▪         Vapor pressure

▪         Sublimation and the phase diagram of water

▪         The heat of sublimation of ice

▪         Rate processes in freeze drying – heat transfer and mass transfer

▪         States of matter – crystalline and amorphous


Section 3: Lyo-cycle phases

▪         Freezing (with optional annealing)

▪         Primary drying (sublimation of water vapor)

▪         Secondary drying (diffusion and evaporation of water that did not freeze as ice)


Section 4: Lyo formulations

▪         Excipients for small and large molecules


Section 5: Quality product attributes

▪         General and specific to freeze-dried products

▪         Influence of collapse and eutectic melting

Who are the probable beneficiaries?

▪         Specialists in Quality Control

▪         Chemical Engineers

▪         Production Supervisors

▪         Chemists

▪         Validation

▪         Chemical Engineers

▪         R&D Groups

▪         Equipment Maintenance

▪         Biochemists, Pilot Plant Operators

▪         Mechanical Engineers

▪         Quality Assurance Professionals

The course will also benefit those in other departments who find lyophilization among their tasks.

Pharma Faculty Lisa Hardwick Thompson

Lisa Hardwick Thompson 

Pharmaceutical Lyophilization Expert at Lyo Blackboard LLC

Nashville, Indiana, United States

Lisa Hardwick Thompson is a pharmaceutical technology consultant and educator with quality, regulatory, product/process development, and technical management experience at Cook Medical, Baxter, Catalent, and start-up businesses. During her career based in the pharmaceutical CMO sector, her expertise has been dedicated to the creation and/or transfer of clinical and commercial formulations and processes, specifically focused on lyophilized parenteral drug products. Her current role at Lyo Blackboard is devoted to consultation and education in the field of lyophilization.

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RAPS - This course has been pre-approved by RAPS as eligible for up to 4 credits towards a participant's RAC recertification upon full completion.

World Compliance Seminars (WCS) is a Regulatory Affairs Professional Society (RAPS) RA Professional Development Portal provider. World Compliance Seminars is committed to enhancing the ongoing professional development of regulatory affairs professionals and other stakeholders through appropriate regulatory affairs learning activities and programs. World Compliance Seminars has agreed to follow RAPS-established operational and educational criteria