PDA

You have been chosen to receive this valuable information.

PDA Annual Pharmaceutical Microbiology Conference Training Course Series
Oct. 25, 2019 | Rockville, MD

Following the 14th Annual PDA Global Conference on Pharmaceutical Microbiology, build on your learning experience and extend your stay so you can bring practical, applicable skills back to your facility.

Gain the knowledge and understanding you need to improve product quality with these eight training courses, offered as part of the PDA Annual Pharmaceutical Microbiology Conference Training Course Series.

Validation of Moist Heat Sterilization Processes: Cycle Design, Development, Validation and Ongoing Control
This training course will provide a foundational understanding of sterilization science (microbiology and thermal science) that will then be applied in the selection of a cycle design approach, sterilization process development, process performance qualification and ongoing process control.

Establishment of a Risk-Based Environmental Monitoring Program
Review routine environmental monitoring (EM) program requirements, EM program qualification requirements, use of risk tools for determination of microbial contamination sources in production environments and processes, and EM risk assessment tools and how to use them to create risk-based EM programs.

Application of Quality by Design and ICH Q9 Rules to Aseptic Processes and Their Impact to Sterility Assurance
Learn how to better use and interpret the ICH Q9 and Quality by Design (QbD) Guidelines for application in and improvement of aseptic processes.

Developing a Microbial Monitoring Plan and Leveraging New Technologies for Effective Sterility Assurance in Aseptic Processes
Gain an understanding of the tools, rationales, and guidelines for designing a strong cleanroom microbial monitoring plan and for leveraging/introducing new technologies for effective sterility assurance in aseptic processes.

Contamination Control, Clean Room Design, and Environmental Monitoring for Controlled Environments - Option 2
Learn how design, control, and monitoring work together to provide the required manufacturing environment. Using this knowledge, you will be able to identify opportunities for improvement within your own companies.

Exclusion of Objectionable Microorganisms from Pharmaceutical and OTC Drug Products
This training course, derived from the work of the PDA Objectionable Microorganism Task Force, will provide guidance on how to manage the microbial risks associated with objectionable microorganisms within a specific product that meet the microbial limit requirements for release to the market.

The Microbiology of Water in a GMP Environment
This interactive training course will examine a variety of the issues surrounding water in a facility to include the testing of each water source, testing requirements during commissioning, and testing on an on-going basis.

Identification of Fungi for Quality Control
This one-day training course will provide participants with the information necessary to establish an in-house identification program for fungi (molds and yeasts), resulting in substantial savings for their companies. Discussions will include principles of basic mycology and the macro- and microscopic examination of fungi.

Visit pdatraining.org for a complete list of PDA training courses.

PDA is an accredited provider of continuing education, offering high-quality, relevant training for both new and experienced professionals working in industry, government (health authority), and academia.

The Parenteral Drug Association (PDA) | 4350 East West Highway | Bethesda, MD 20814 USA

Message above is a paid advertisement. Content is provided by the sponsor. You received this email because you are a customer of BioPharm International, a UBM publication. You are on the mailing list as %%emailaddress%%.