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Analysis & Testing (QLP Module 7)

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A fundamental part of the product release decision is the review and interpretation of analytical data.

Tuesday 04 to Thursday 06 December 2025
Royal Sonesta Hotel Boston, MA, USA

$2950.00 per delegate
$2360.00 for additional delegates from same site or early bird booking

Type: Pharmaceutical

Book now PDF brochure

About this course

A fundamental part of the product release decision is the review and interpretation of analytical data. It is therefore essential that the Technical and Quality Leader understands the basis of the analytical techniques and their respective strengths and weaknesses.

This course seeks to provide a foundation of knowledge to enable the Quality Leader to judge analytical data, to be able to ask relevant questions to aid interpretation and to know when to call for additional data/advice.

The module is designed for delegates with a scientific background who wish to obtain a broader knowledge of Good Control Laboratory Practice (GCLP). The module may also be suitable for Analytical Chemists and Biochemists who are new to the Pharmaceutical Industry.

For delegates who already have a deeper knowledge of analysis and testing there will be opportunities to discuss issues with the course tutors

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.

Continuing Education Credits

ACPE Continuing Education Units = 3.0 CEUs
Reference Activity Number 0616-9999-12-003-L04-P

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