PDA Training and Research Institute Adds 31 Courses to GSA Schedule
PR Newswire Association LLC |
The 31 courses will be included on the GSA Advantage, GSA's online shopping and ordering system https://www.gsaadvantage.gov/advantage/main/start_page.do). This will improve the visibility of these PDA TRI courses to federal officials and make it easier for them to participate. Over the years, PDA TRI has conducted numerous training courses specifically designed for officials at the
"By adding 31 courses to the GSA Federal Supply Schedule, employees of the U.S. Federal Government will have an easier time participating in the unique, world class training courses in the PDA TRI facilities and lecture courses," says PDA President
The courses are listed under Special Item Numbers (SINs) 874-4: Training Services. They are:
- An Introduction to the Advanced Molecular Methods for Virus Detection
- An Introduction to Visual Inspection
- Aseptic Processing for Senior Management
- Aseptic Processing Training Program
- Biosimilars - Understanding the Challenges of Meeting 'Similarity'
- CMC Regulatory Requirements in Drug Applications
- Evaluation, Validation and Implementation of Alternative and Rapid Microbiological Testing Methods
- Filters and Filtration in the Biopharmaceutical Industry – Basics Course
- Filters and Filtration in the Biopharmaceutical Industry – Basics Course and Advanced Course
- Filters and Filtration in the
Biopharmaceutical Industry – Advanced Course - Fundamentals of an Environmental Monitoring Program
- Fundamentals of Aseptic Processing
- Fundamentals of Cleaning and Disinfectant Programs for Aseptic Manufacturing Facilities
- Fundamentals of Lyophilization
- Fundamentals of Lyophilization and Validation of Lyophilization
- GMPs for Manufacturers of Sterile and/or Biotechnology Products
- Implementation of Quality Risk Management for Commercial Pharmaceutical and Biotechnology Manufacturing Operations
- Implementing Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations:
Case Studies in the Manufacturing of Biotechnological Bulk Drug Substances - Implementing Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations:
Case Studies in the Packaging and Labeling of Drug Products - Implementing Quality Risk Management for Pharmaceutical and Biotechnology Manufacturing Operations:
Case Studies in the Manufacturing of Pharmaceutical Drug Products - Investigating Microbial Data Deviations
- Microbiological Quality of Raw Materials and Components
- Microbiological Risk Assessment of a Pharmaceutical Manufacturing Process
- Preparation of Virus Spikes Used for Virus Clearance Studies and Virus Filtration
- Quality Systems for Aseptic Processing
- Risk-Based Qualification of Sterile Drug Product Manufacturing Systems
- Single-Use Systems for the Manufacturing of Parenteral Products
- Validation of Biotechnology-related Cleaning Processes
- Validation of Dry Heat Processes Used for Depryogenation And Sterilization
- Validation of Lyophilization
- Virus Contamination in Biomanufacuring: Risk Mitigation, Preparedness and Response
About PDA – Connecting People, Science and Regulation®
About
Media Inquiries:
Logo - http://photos.prnewswire.com/prnh/20130226/DC66667LOGO
SOURCE
Wordcount: | 625 |
Advisor News
Annuity News
Health/Employee Benefits News
Life Insurance News