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HPLC Analytical Method Development Validation

This two-day course provides comprehensive training on developing and validating HPLC analytical methods for drug substances and products. The course will cover method development, optimization of separation conditions, and validation according to ICH guidelines. Attendees will learn how to select separation modes, columns, mobile phases and detectors to develop methods and how to validate method parameters including specificity, linearity, accuracy and precision. The course is designed for scientists who develop and validate HPLC methods for quality control, stability testing and regulatory submissions.

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Joshua Castillo
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© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
246 views

HPLC Analytical Method Development Validation

This two-day course provides comprehensive training on developing and validating HPLC analytical methods for drug substances and products. The course will cover method development, optimization of separation conditions, and validation according to ICH guidelines. Attendees will learn how to select separation modes, columns, mobile phases and detectors to develop methods and how to validate method parameters including specificity, linearity, accuracy and precision. The course is designed for scientists who develop and validate HPLC methods for quality control, stability testing and regulatory submissions.

Uploaded by

Joshua Castillo
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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HPLC Analytical Method Development and Validation

24 & 25 November 2014 - London UK


8 & 9 June 2015 - Amsterdam NL
Overview
Analytical methods must be validated to provide reliable data for regulatory submissions.
These methods are essential for a number of purposes, including testing for QC release,
testing of stability samples, testing of reference materials and to provide data to support
specifications.
This course provides a comprehensive coverage of the method development and
validation requirements that are essential to progress a pharmaceutical compound, at
each stage of product development.
Upon completion of this course, delegates will have learned what is necessary to develop
and validate methods for drug substance and drug product to comply with international
regulatory guidelines.

The course is designed for

Scientists working with HPLC who need to further their understanding of the technique in
order to develop better methods faster. Scientists who have to validate HPLC methods in
accordance with current internationally-accepted guidance. HPLC technicians working in
R&D laboratories, quality control laboratories and stability testing laboratories.
Managers with a responsibility for generating regulatory submissions.

Speaker:

Dr Roland Collicott, as an exp erienc ed c onsultant and trainer, pro vides assistance to
the pharmaceutical industry in the areas of chiral analysis , polymorphic characterisation,
stability studies, chemical analysis in a GMP environment, specifications and all aspects of
international CMC documentation. He also runs training courses to cover many areas of
analytical chemistry, particularly in chromatography, chiral and polymorphic analysis. He has
served as an expert witness and consulted in trials in Canada, UK, South Africa and Germany.
Before becoming a consultant Roland was analytical section manager at OSI Pharmaceuticals
responsible for delivering validated analytical chemistry methods and CMC documentation for
OSIs regulatory submissions. In this role, he was responsible for collating and interpreting
data from a wide range of analytical techniques, acquired in-house or at contract, for the
characterisation of new compounds. There he also gained valuable international experience,
working closely with regulatory and clinical groups as well as manufacturing and analytical
contractors in Asia, Europe and the US.
Roland began his career in physical chemistry at Glaxo Group Research and originally
specialised in chromatography, introducing the use of chiral HPLC columns to resolve
enantiomers. He gained a PhD from his research into novel silicon-based chiral derivatisation
reagents for HPLC, GC and NMR analysis. In 1998 he joined British Biotech, where he became
involved in many other areas of analytical chemistry including polymorphism in pharmaceutical
products. As Group Leader, he managed British Biotech's QC procedures, stability testing and
the analytical development of its NCEs.

www.pharma-training-courses.com

HPLC Analytical Method Development and Validation


24 & 25 November 2014 - London UK
8 & 9 June 2015 - Amsterdam NL
Course Programme
Day One

Analytical method development, part 1


Theory and factors affecting resolution - a reminder of the importance of
resolution, separation factor (selectivity), retention factor (capacity
factor) and column efficiency).
Selecting the HPLC separation mode (reversed-phase, normal-phase
etc.)
Overview of instrumentation
Selecting the most appropriate detector
Troubleshooting
Workshop: Selecting the separation mode
Analytical method development, part 2
Selecting the column for analysis
Scouting runs as a guide to optimum conditions
Using chromatographic parameters to decide quality of chromatography
Gradient/isocratic operation appropriate?
Selecting and optimising the mobile phase
The effect of pH, considering pKa of the analyte
Workshop: Selecting the column and mobile phase
End of Day One: Group discussion

Day Two

Validation of chromatographic methods, part 1


Introduction to ICH guidelines: ICH Q2(R1)
Types of analytical procedure to be validated:
Identification test *Quantitative test (impurities content)
Limit tests (control of impurities)
Quantitative test of active moiety (assay vs. external standard)
A detailed discussion on the parameters to be validated:
Specificity: peak purity determination (Diode array and MS detectors)
Linearity
Range
Accuracy
Precision
Detection Limit
Quantitation Limit
Robustness
Workshop: Validating a typical HPLC method
Validation of chromatographic methods, part 2

Comparison of the traditional and Quality by Design (QbD) approach to


validation

Extent of validation: how much work at each phase of development?

Acceptance criteria

Validation procedures and protocols

Dealing with validation failures

Verification of compendial procedures


Workshop: Dealing with validation failures and
how to avoid failures
End of Day Two: Group discussion and close

Venues:
Amsterdam: Hotel Amsterdam, Damrak 93-94, Amsterdam 1012LP, Netherlands
Phone:+31(0)20 555 06 66
Website: www.hotelamsterdam.nl
London: DoubleTree Hilton, (formerly Jurys Inn) 60 Pentonville Road, Islington
London N1 9LA
Website: www.doubletree3.hilton.com
Accommodation and travel directions are available on our website

www.pharma-training-courses.com
For 5 or more staff requiring training it may be beneficial to run a course in-house.
The benefits of running a cou rse in -house:
Save on travel or accommodation costs
Customised content to meet your requirements
Big print savings on course material - especially with larger groups
Courses arranged for large groups up to 24 staff
Tutorials available for small groups of 2 or 3 staff
Meet course speakers in advance to discuss design and content
Contact Judy Callanan at any time to discuss
Ph: 0044 (0)20 7193 7703, Email: judy@pharma-training-courses.com

PharmaCourses Ltd
Suite 1327 Kemp House
152 City Road
London
UK
Tel: ++44 (0)20 71937703
Email: info@pharma-training-courses.com

Keep up to date with industry requirements

REGISTRATION DETAILS:

HPLC Analytical Method Development and Validation


24 & 25 November 2014 London, United Kingdom
Early-bird fee: 2 day course 1062.00 (+ VAT 212.40 if applicable, see notes on VAT)
For registering and paying before 30 September 2014
Full Fee: 2 day course 1180.00 (+ VAT 236.00 if applicable, see notes on VAT

8 & 9 June 2015 Amsterdam NL


Early-bird fee: 2 day course 1080.00 (+ VAT 216.00 if applicable, see notes on VAT)
For registering and paying before 10 April 2015
Full Fee: 2 day course 1200.00 (+ VAT 240.00 if applicable, see notes on VAT

UK: Under UK law all UK-based applications are subject to VAT at the prevailing rate however most UK VAT
registered companies/organisations can reclaim this tax.
EU: With effect from 1 January 2011 applications from delegates whose companies are based in EU countries will not
be subject to VAT PROVIDED THAT valid VAT ID details are provided at the time of booking, otherwise VAT will
be charged.
OTHER: With effect from 1 January 2011 applications from delegates whose companies are based outside of the UK/
EU will be outside the scope of VAT, ie no VAT is charged or payable.

Methods of Payment available:


Cheque (Please make payable to PharmaCourses Ltd)
Bank transfer
Credit/Debit Card (If paying by Credit Card please register online)

Online Registration is available on our website:


www.pharma-training-courses.com
Data Protection
PharmaCourses Ltd gathers personal data in accordance with the UK Data Protection Act 1998
and we may use this to contact you by telephone, fax, post or email to tell you about other
products and services. If you have any queries or want to update any of the data that we hold then
please contact us.
Terms and Conditions: Delegate fees: Fees for this programme are shown overleaf. Delegate
fees are inclusive of course documentation, refreshments and lunch. Payment of the registration
fee must be paid within 14 days of commencement of the course. Upon receipt of payment, a
proof of payment will be sent to you. Cancellation Policy: Full refunds less a handling fee of
100 will be made for cancellations received in writing within 28 days of the commencement of
the course. Refunds of 50% will be made for cancellations received in writing between 28 and 7
days prior to the commencement of the course. Regrettably no refunds will be made after 7 days
prior to commencement of the course. Substitutions can be made at any time.
Liability: PharmaCourses Ltd reserves the right to change the
programme, speakers, date or venue without notice or cancel the
PharmaCourses Ltd
event. If cancellation occurs delegates will be notified as soon as
Suite 1327 Kemp House
possible and will receive full refund of fees paid. PharmaCourses Ltd
152 City Road
will not be responsible for any airfare, accommodation or other travel
London
costs incurred.
UK
PharmaCourses Ltd is Registered in England and Wales No. 08509096

Tel: ++44 (0)20 71937703


Email: info@pharma-training-courses.com

www.pharma-training-courses.com

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