An NSF International Company Pharmaceutical Analysis and Testing (QLP Module 7)
PrintA fundamental part of the product release decision is the review and interpretation of analytical data.
$2950.00 per delegate
$2360.00 for additional delegates from same site or early bird booking
About this course
A fundamental part of the release decision is the review and interpretation of analytical data. It is therefore essential that those responsible understand the basis of the analytical techniques and their respective strengths and weaknesses.
This course seeks to provide a foundation of knowledge to enable individuals to judge analytical data, to be able to ask relevant questions to aid interpretation and to know when to call for additional data/advice.
This course is designed for delegates seeking to stay current on Good Control Laboratory Practice (GCLP) or wishing to deepen their knowledge of pharmaceutical laboratory operations. The scope will encompass analytical method validation and method transfer – both relevant to typical small molecules analytical testing and methods commonly used to test biologics. In addition, regulatory agency focus regarding method validation issues, out-of-specification handling, and data integrity will be covered.
Continuing Education Credits
ACPE Continuing Education Units = 3.0 CEUs
Reference Activity Number 0616-9999-12-003-L04-P
How This Training will Benefit You
Analysis and Testing represents a key element for the Quality Leader and the Technical Professional. This course provides the tools and techniques required to make informed, science and risk based decisions to benefit both the business and the patient.
It will provide the background and knowledge needed by every Quality Professional and Technical Leader whether in Production, Quality, R&D, Validation, Engineering, or any other technical discipline. As with all of NSF-DBA’s courses, it is led by industry and academic experts; frequently incorporating case studies and small group sessions to facilitate learning.
NSF-DBA’s format of extended days and pre-work ensures that both you and your company benefit from the learning experience in an efficient way and with minimal time away from the workplace.
This course on Analysis and Testing is based upon a key component of the Qualified Persons instruction which NSF-DBA offers in Europe. It sets a new standard for practical, results oriented instruction.
A Certificate is granted by NSF-DBA for attendance. Higher degree options – a Diploma and a Masters in Pharmaceutical Quality and Good Manufacturing Practice from the University of Strathclyde can be obtained by attending a full series of courses.
