The pressure has been mounting in the pharma and biopharma industries in recent years to do more with less. Analytical laboratories are no exception to this trend. Work piles up while personnel have been cut or remain stagnant. Accelerated timelines further strain resources. Constant firefighting and band-aiding results in errors as well as compliance violations. It can be argued that the cost of non-compliance is more than that of compliance.
Areas Covered in the Seminar:
Upon completing this course participants should be able to:
Understand what the global best PM practices are for analytical testing laboratories
Utilize a systematic risk based approach to developing an effective and scientifically justified method development, validation and technology transfer process
Evaluate effectiveness, suitability and adaptability of Gantt charts, Excel work sheets and other planning tools to increase lab efficiency
Who will Benefit:
This course is designed for people tasked with developing, validating, maintaining and/or improving testing methods for pharmaceutical or biotechnology industries. This includes individuals that have Quality Control Laboratory responsibilities or method development responsibilities for small molecules or biologics. Anyone with a testing lab responsibility interested in making general improvements in their organization’s performance specifically related to efficiency, productivity or compliance can benefit. The following personnel is a sampling of who will benefit from this course:
Senior Analytical managers
Quality Control/Assurance professionals
Regulatory professionals
Compliance professionals
Laboratory supervisors
Process owners
Note:
Use coupon code NB5SQH8N and get 10% off on registration.
For Registration:
http://www.complianceonline.com/project-management-tools-to-improve-productivity-and-compliance-in-analytical-laboratories-seminar-training-80316SEM-prdsm?channel=sciencedz