Webinar Includes : All the training handouts , certificate ,Q/A and 60 mins Live Webinar
Who will Benefit
- Manufacturing Personnel (Associates and Supervisors) and Managers.
- Quality Control Personnel (Associates and Supervisors)
- Quality Assurance Personnel (Associates and Supervisors)
- New Graduates just entering into the Pharmaceutical Manufacturing Industry
- Easy to understand
- Make sure others read the document
- Technically accurate
- Equipment names
- QA sign off
- QA input
- Structure of document meets requirements
- Case Study 1
- Case Study 2
- Case Study 3
These module will provide insight into what the FDA is looking for during an audit and provide participants with tools and case studies for each of the topics.
Why Should You Attend
The FDA is a regulatory body that can shut down a manufacturing facility then the company loses time and money due to the closure. For this webinar series, we are providing the most common observations given by the FDA and provide ways to prevent these most common observations.
Industries who can attend this training
This 60-minute online course is intended for professionals in the Pharmaceutical, Clinical Data Management SaaS companies, and medical device companies . Although not presently stated in the draft , the same guide could be used by FDA Regulated Industries personnel.
Faculty Carl Patterson
Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However, his avid interest in all things biology, microbiology, and biochemistry officially began when he served in the U.S. Army as a Preventative Medicine Specialist and a Licensed Vocational Nurse.