Dry Powder Inhalers II: Enhancing bioavailability through product design

Instructor: Claudio Cerati
Product ID: 702013
  • Duration: 85 Min

Training CD / USB Drive

One CD/USB is for usage in one location only.
(For multiple locations contact Customer Care)
CD/USB and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-362-2367


Read Frequently Asked Questions

This webinar on Dry Powder Inhalers will focus on pharmaceutical active particle design, physical characteristics and its relationship with product behavior both in vitro and in vivo.

Why Should You Attend:

Drug action when delivered through a dry powder inhaler device is closely related to both physical considerations and chemical interactions between the interface, between well defined inhaled particles and the respiratory tract surface . Many patented products developed in this area takes into account the spherical shape and also hollow characteristics of carrier particles.

No attempts have been made till now to combine a carrier with usual aerodynamic diameter and develop active spherical particles that can be adhered to the carrier with and adhesion force similar to those obtained with a traditional powder mix. Impact on bioavailability is in close relationship with both carrier and active particle design and formulation.

In this webinar we will analyze the interaction of new product design and both usual impactor equipments and drug delivery devices.

Areas Covered in the Seminar:

  • API particle size and shape.
  • How to control those parameters.
  • Formulating spherical particles.
  • Optimizing formulations to achieve reproducibility.
  • Strategies to enhance drug bioavailability.
  • Device and product impact on bioavailability.
  • Understanding in vitro testing and relating to in vivo results.

Who Will Benefit:

This webinar will provide a valuable point of view for those professionals working in the field of Dry Powder Inhalers and inhalator drug delivery systems. Professionals who will benefit include

  • R&D Professionals
  • R&D Technical people
  • New Product Project Developers
  • Pharma Production Professionals
  • Consultants

Instructor Profile:

Claudio Cerati , is an independant consultant in the pharmaceutical industry was Director of Research and Development Department at Tecnoquimicas SA in the city of Cali, Colombia and in Pharmaceutical companies in Argentina (Phoenix Laboratories ). During the last twenty five years , he was directly involved in R&D, Quality Control and Manufacturing areas in national and multinational companies in latin américa ( Argentina and Brazil) with the direct responsibility of developing and scaling up pharmaceutical processes.

Follow us :
Latin America: Regulatory Compliance Requirements for Life Science Products
Upcoming In-person Seminars by EX-FDA OFFICIALS

Refund Policy

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.

If you have any concern about the content of the webinar and not satisfied 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 call +1-888-717-2436 (Toll Free).

Product Reviews

This product hasn't received any reviews yet. Be the first to review this product! Write review

Best Sellers
You Recently Viewed