Quality Control of Raw Materials (APIs and Excipients)

Quality Control of Raw Materials (APIs and Excipients)

Copenhagen, Denmark

Course No 9150


Costs

This conference already took place.

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@gmp-compliance.org

Speakers

Emerich Grassinger, Haupt Pharma Wülfing
Armin Groh, Takeda
Dr Reto Theiß, Merck
Dr Thomas Storm, Novartis Pharma

Background

Testing active pharmaceutical ingredients and excipients is one of the main tasks of the quality control units in the pharmaceutical industry. It must be ensured that the necessary tests are conducted on the incoming goods and that the starting materials are released only after their quality was judged as satisfactory. This GMP Education Course about the incoming goods control of APIs and excipients will give you a comprehensive overview of the specific tasks and questions of the „raw materials lab“ and show you real-life solutions and answers.

This course will deal among others with the following questions:

Who is responsible for the release or rejection of starting materials?
How can the incoming goods lab be organised efficiently?
Which SOPs are necessary?
In which cases can test results be taken over from the supplier‘s certificate of analysis?
Do all test items of a pharmacopoeial monograph have to be analysed?
Are the pharmacopoeial monographs similar, or must different tests be conducted for PhEur, USP and JP?
Can a pharmacopoeial test method be replaced by an alternative test method? Does this require a variation application?

It is the aim of this GMP Education Course to give answers to these and many other important questions relating to the testing of APIs and excipients and to serve as a forum for an intensive experience exchange.

Target Group

This Education Course is directed at all those employees from quality control units in the pharmaceutical industry (including heads of quality control and laboratory managers) who are competent or responsible for sampling, testing and release of the starting materials used (= APIs and excipients).

This course is also of interest to personnel from quality assurance and to those employees from API and excipient manufacturers who want to inform themselves about the requirements of the pharmaceutical industry on the testing of these starting materials.

Programme

Regulatory Requirements for APIs and Excipients
Definition of APIs and excipients
EU Requirements
FDA Requirements, e.g. FDA Draft Guidance “Drug Product”
Common Technical Document (CTD)
Certification Procedures:
- EDQM Certificate of Suitability
- Active Substance Master File
- US - Drug Master File
Quality Standard: How to discern a good starting material from a bad one?

Current GMP Requirements for APIs, Excipients and Drug Products
Relevant ICH guidelines
EU regulations for Drug Products and API
GMP for excipients – current expectations
IPEC (International Pharmaceutical Excipients Council) Guideline for excipients
Upcoming EU GMP regulation for excipients
GMP aspects of supplier/manufacturer qualification

Laboratory Organisation
Role of the raw materials laboratory within the pharmaceutical supply chain
Optimization of the analytical laboratory with respect to costs, time and resources (economic order size, costs of analysis vs stock keeping costs, involvement of RM suppliers in the SC)

Pharmacopoeias
Regulatory background
Pharmacopoeial institutions – Ph.Eur., USP/NF, JP
CEPs
Implementation of pharmacopoeial monographs in your laboratory
Multi-compendial testing
Validation of pharmacopoeial testing methods
New USP General Chapter <1226> Verification of Compendial Methods

Sampling of Incoming APIs and Excipients
Regulatory requirements
Are the requirements the same for active and excipients?
Sampling plans
Training
GMP-compliant documentation of sampling operations
Practical examples

Reduced Testing of Supplied APIs and Excipients
What guidance is available on reduced QC testing?
EU and FDA expectations?
Supplier qualification as a prerequisite
Other information required before you start reducing
Can APIs and excipients be covered within the same approach?
Who is in the driver seat, who must be involved?
Practical execution

Analytical Methods
Use and validation of non-compendial methods
How to proof comparability?
Advantages of instrumental methods versus visual methods
Handling of deviations (Out-of-Specification results and complaints)
CAPA process
Measurement system analysis
Documentation
Retests

NIR (Near InfraRed Spectroscopy) for an Efficient
Control of Raw Materials
A short introduction to NIR Spectroscopy
NIR as a pharmacopoeial monograph
NIR for single container identification
Costs vs. benefit
NIR vs. ATR

WORKSHOP II
Reduced Testing
Apart from any guidance, it is still much up to the manufacturer to decide which APIs and which excipients might be subject of a reduced testing procedure. Since the quality of the substance has to be assured without compromise, multiple factors must be considered before the full testing of every single batch can be reduced. It is the aim of this workshop to exchange information about different approaches and to discuss their advantages and disadvantages respectively considering the actual guidance as well as their practicability.

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