Cannabis Formulation/Product Development Strategies for Medical/Recreational Oral Dosage Forms


Instructor: Moe Harati
Product ID: 706582
Training Level: Intermediate to Advanced

  • Duration: 90 Min
Successful cannabis product development requires having the-end-in-mind regarding excipients-cannabinoids compatibility, shelf-life/product stability and bioavailability of cannabinoids. This webinar will utilize presenter’s expertise and experience in both pharmaceutical and cannabis industries to provide guidance and examples on successful product development. You will learn various techniques to successfully initiate and optimize formulation for products containing cannabinoids.
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Why Should You Attend:

Cannabis industry can learn from a well-established pharmaceutical to develop a successful product with optimized formulation and subsequently longer shelf-life. This workshop will utilize presenter’s 20+ years’ experience in leading various pharmaceutical and cannabis companies research and development’s teams. The Goal of this workshop is to provide participants with concepts, tips and tricks of things to do and not to do for a successful quick product development to either enter recreational market or quick ANDA submission to FDA or other regulatory agencies.

We will explore risk-based evaluation of product quality and impact of excipients

Concept and application of quality by design including critical material attributes (CMA) and critical process parameters (CPP). Planning for excipient-cannabinoids compatibility will be explored in a generic format expandable to specific applications.

Various oral dosage forms will be reviewed including capsules, gummies, emulsions and tables. Fill and shell formulation and compatibility for capsules will be explored with discussing various types of fill formulations.

The following questions will also be answered: What is the role of excipient in a formulation? What is the relationship between Dissolution/disintegration and bioavailability of cannabinoids? What are different scenarios for release of cannabinoids?

As part of this workshop, literature review, quality target product profile (QTPP) and concept of Quality Attributes (CQA) will be linked to proof-of-concept, i.e., bench work and comparable properties of product such as dissolution and disintegration.

Areas Covered in the Webinar:

  • Design of experiment
  • Role of excipients
  • excipients-cannabinoids compatibility
  • shelf-life
  • product stability
  • bioavailability
  • quality by design
  • critical material attributes
  • critical process parameters
  • quality target product profile
  • concept of Quality Attributes
  • Dissolution and disintegration

Who Will Benefit:

  • Formulation Scientists
  • Analytical Scientists
  • Research and Development Scientist/Chemist
  • Chemists
  • Quality Control Chemist
  • Lab Technicians
  • Product Development Managers/Directors
  • Product development Chemist

From all industries, service and manufacturing companies working in cannabis and pharmaceuticals.

Instructor Profile:
Moe Harati

Moe Harati
Technical Director, Pharmaceutical Industry

Dr. Harati is an expert and leader in pharmaceutical and cannabis industries with a broad research background and training in business administration that makes him able to quickly recognize challenges and provide clear, effective solutions. He has broad experience in research and development, product development, CMC product development, strategic planning and continuous improvement.

Dr. Harati is a high energy, tenacious leader that engages and inspires the team to own and execute the business plan with excellence. Over the past 20+ years, he has successfully led technical teams to develop novel products and analytical testing from discovery to commercialization. He facilitates fundamental product and process understanding and the advancement of innovative approaches to pharmaceuticals and cannabis development. Dr. Harati is author and presenter of more than 100 conferences, technical summaries, publications, funding white papers, and training guides.

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Refund Policy

Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).




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