Pharma / Biotech
Efficient and effective batch record reviews provide pharmaceutical companies with two strategies. First, reviews are key to maintaining control of your firm's operations, eliminating any guesswork and aiding in the resolution of atypical occurrences. Secondly, they enable a company to maintain and demonstrate a compliant posture - a sure way to avoid any quandary with the regulatory agencies.
This course is intended to take the mystery out of the batch record review process. The class examines the FDA and EU regulatory requirements for documentation and batch record reviews, explains the elements of the batch record review process, and clarifies the pathway to effective deviation investigations. Interactive sessions are included for identifying reviewer responsibilities, establishing good documentation practices, and writing procedures for the review process. Additionally, participants will be able to analyze their company's compliance with these requirements and identify missing elements of the batch review process.
Ample time is provided to address specific problems and questions of individual participants. Additional benefits of this class include:
This two-day course is designed for pharmaceutical production, quality assurance and compliance personnel who are responsible for the review and audit of production batch records, and batch record deviation investigations. This includes, but is not limited to, such positions in Quality Control, Quality Assurance, Manufacturing, and Packaging groups. Those who supervise, manage, or oversee these activities would also benefit from this program.
Upon completion of this course, attendees will gain a clear understanding of the batch record review expectations of regulatory agencies and discover the elements of an effective batch record reviewer training program. Participants will learn how to prepare for a technical review of batch records, as well as how to measure the effectiveness of the review process. In addition to recognizing what to do when a batch fails to meet specifications (deviations), how to determine deviation cause, and corrective and preventive action(s) (CAPA), learners will see the benefits of a working relationship between production and quality reviewers.
"This was an excellent course. I highly recommend it. I definitely have a few new ideas/concepts to present to my place of employment." Michael B., Quality Assurance Auditor, Colorcon
"Great course, even for a person who has reviewed batch records for years. This was a wonderful, refresher course with useful, helpful information that I can take back to my company and incorporate into our processes. Thank you!" Dana F., QA Specialist, Morphotek
"I really appreciated the manner of engagement the course director brought to our course as a facilitator. He truly took on the dual roles of instructor and facilitator. We had great discussions and dialogue with our other class participants and wonderful opportunities to share our experiences in an open but confidential forum." Jenifer G., Document Specialist, Catalent Pharma Solutions
"The course was very enjoyable, interesting, and the information was presented clearly. I have gained many tips from this course, which will help me in the future when carrying out GMP audits, where BR review is such an important aspect. The information shared between all the attendees was very valuable. It's always great to get actual experiences that relate to my own situation." Clodagh O., QA Manager, Cambridge Laboratories
"This course took me one step further in my career and pharmaceutical practice. It was very interesting, beneficial and enjoyable. I strongly recommend this course for my colleagues who are working in production review and QA. Thank you." Haidar A., Head of Production, PHARMASPEC
"Best and most informative course I've ever taken! Information was presented in such a way that the material will stick with me for quite some time. The Course Director was excellent!" Charles F., Manufacturing Supervisor, Novovax
"The course was excellent! The hands-on exercises used were by far the most practical I've experienced in such a course. I am leaving this two-day course with several deliverables that I can now implement within our group." Mary S., Quality Assurance Manager, BioMARC
"The course director was very pleasant, well prepared, helpful and encouraged regular interaction. He had everyone engaged and broke the course up well to keep it fresh. He also allowed us to give our expectation up front so that we could get what we wanted from the course. I enjoyed this course and the course director was very nice." David C., Manufacturing Team Leader, Genzyme
"I really appreciate leaving the class with a working document (SOP). Capturing students in their purest form of "think mode" is a wonderful idea & concept." Marney F., Compliance Specialist, Nutrilite
The material covers both the 21CFR and the Eudralex Vol. 4 content regarding the activities surrounding the batch record review including but not limited to reviewing all production batch records and making sure that all production deviations are reported and evaluated. Most often, class participants share their techniques for handling errors In addition to the instructor reviewing the handling of errors.
The creation of EBRs and their relationship to an electronic manufacturing environment are presented, as well as a comparison to paper batch records.
In fact, the instructor presents a "best practice" for reviewing batch records and participants actually practice reviewing a record as one of the class exercises.
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*Valid up to 30 days prior to course date(s). Cannot be combined with other discounts or offers.
The Center for Professional Innovation and Education (CfPIE) provides technical training for Pharmaceutical, Biotech, Medical Device and Skin/Cosmetics professionals. CfPIE offers more than 350 class sessions annually across 80 course titles in multiple formats, such as classroom, on-site and certification programs.
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