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ComplianceOnline, Online Event
2012-11-28
Why Should You Attend: Learn practical strategies for improving productivity in Pharmaceutical Laboratories, including Quality Control, Research and Development and Stability laboratories. The presenter will pull from a wealth of experience to address selection and development of personnel, establishment and pursuit of goals to reduce ‘waste’ and increase productivity, and smart use of automation and computerization.
Upon completion of this course the learner will be familiar with a proven strategy to: - Get the most out of the employees in your lab.
- Use training and personnel development to improve your technical expertise.
- Establish laboratory goals improve productivity and turn-around time and reduce investigations
- Streamline processes and use computer templates to speed things up.
- Begin to decide if lab computer systems (chromatography, LIMS, electronic notebook) are right for your lab.
Interaction and questions from the participants are actively encouraged, and there will be ample time for questions at the end of the presentation. Areas covered in this webinar: - Introduction: Responding to the Demand for ‘More from Less’
- Your greatest resource: people
- Strategies to hire the right people
- Inexpensive ways to increase motivation
- Making sure staff have the right training
- Establishing goals for the laboratory.
- Improving processes to decrease turn-around time
- Reducing the need for investigations
- Using computerized templates to make documentation simpler
- Practical examples
- Smart pursuit of automation and computerization
- Setting the stage for success
- Automated equipment
- Computerized laboratory systems: chromatography, LIMS, notebooks
- Practical examples
- Questions
Who Will Benefit: - Laboratory supervisors
- Laboratory managers
- Laboratory directors
- IT/IS
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Organized by:
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Complianceonline |
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Invited Speakers:
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Greg Martin, is President of Complectors Consulting which provides consulting and training in the area of Pharmaceutical Analytical Chemistry. He has particular interest in QbD/Lean approaches to dissolution testing, impurity methods, method lifecycle (development/validation/transfer) and instrument qualification, and is passionate about using good science and sound logic to achieve high quality results, consistent with cGMPs, while minimizing resources. Mr. Martin has over 25 years experience in the pharmaceutical industry and was Director of Pharmaceutical Analytical Chemistry (R&D) for a major PhRMA company for a number of years. In addition, he has volunteered for the USP for over 10 years, and currently serves as Vice Chair of the General Chapters – Physical Analysis Expert Committee, and serves on Expert Panels on Validation and Verification, Weights and Balances and Use of Enzymes for Dissolution Testing of Gelatin Capsules. He is also Chair-elect of the AAPS In Vitro Release and Dissolution Testing Focus Group.
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Deadline for Abstracts:
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2012-11-27
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Registration:
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For Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702533?channel=hummolgen
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E-mail:
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referral@complianceonline.com
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