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Cost Effective – Time Effective –
In your Conference Room or Office
ASTM E2500 Consensus Standard:
An Overview of a New Approach to Validation
Conducted by Gamal Amer, PhD
Principal - Premier Compliance Services, Inc.
June 27, 2008
This seminar will focus on providing an overview of the contents of the
ASTM E2500 consensus standard. This important standard was finalized and
issued in the summer of 2007. Because this is a consensus standard, all
governmental agencies are required by law to accept its premise and abide by
its requirements. So unless an agency chooses to challenge it in court, the
standard will be followed. Both industry and the regulators are still
reviewing it and assessing its potential impact.
The main inputs for developing the standard was to
reduce the cost of validation and simplify the effort for industry. The
standard achieves such an objective through reducing the effort from the
current established commissioning, qualification and validation approach, to
verification followed by validation. The standard further suggests that
verification of equipment and systems’ suitability for the intended use can
be achieved through an overall quality approach, which starts at the
conceptual phase of the project and continues through start-up and
operation. This includes a science and risk- based evaluation to determine
the extent of the effort while utilizing information developed by the
suppliers all under the guidance of Subject Matter Experts (SMEs).
By participating in this presentation you will learn:
- The details of this
new standard and how to apply them
- What is meant by
Verification of suitability for intended use
- How to use a science-
and risk-based approach to ensure the proper verification is conducted
- The importance of URS
(Users Requirements Specifications), GEP (Good Engineering Practice),
QbD (Quality by Design), and SMEs in support of the validation effort
- The differences and
similarity with the current approach to validation
- What’s in store for
the immediate future
In this
unique web seminar format, lasting just one hour, you will be able to follow
along with a PowerPoint presentation, ask questions, and interact
with Dr. Amer. An outline of this seminar and Dr. Amer’s qualifications
can be found below.
ASTM
E2500 Consensus Standard:
An Overview of a New Approach to Validation
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Part I Understanding the new
Standard
- The details of
this new standard and how to apply them
- What is meant
by Verification of suitability for intended use
- How to use a
science- and risk-based approach to ensure the proper
verification is conducted
- The importance
of URS (Users Requirements Specifications), GEP (Good
Engineering Practice), QbD (Quality by Design), and SMEs in
support of the validation effort
- The
differences and similarity with the current approach to
validation
- What’s in
store for the immediate future
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Part II Questions and Answers
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Register now!
Don’t like to order online?
Call us at 714-289-1233
All registrations include handout materials. Once you’re registered, you will
receive via e-mail (the e-mail address you provide in your registration) the web location to download the handout materials.
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dollars.
Note International shipments: If ordering the CD for shipment,
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Get the CD and handout
GMP080627E - CD and
Handout materials
ASTM E2500 Consensus Standard
CD price includes all HANDOUT MATERIALS and audio
CD. CD will be shipped three weeks after the seminar |
$397.00 |
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Instructor
Gamal Amer, Ph.D.
Gamal Amer, Ph. D. is
Principal at Premier Compliance Services, Inc.; Management Consultants for
compliance and manufacturing operations performance in the life sciences
industry. He holds a Ph. D. in Chemical Engineering and has over two decades
experience in the Pharmaceutical and related industries. He has held
positions of increased responsibility with leading pharmaceutical, consumer
product and engineering consulting firms over the years. His experience
includes comprehensive process design in bulk pharmaceutical manufacturing,
biotechnology manufacturing, pharmaceutical solid dosage manufacturing and
containment of potent and radioactive therapeutics. He is also experienced
with facility development for therapeutic products operations.
Dr. Amer is a recognized
expert in GMP compliance and validation. He has consulted for many of the
leading pharmaceutical, biotechnology and medical device manufacturers. He
has lectured extensively in the US, Europe, Asia and the Middle East, taught
many courses, and authored many papers which were published in peer reviewed
publication. He is a member of ISPE, PDA, ACS and AIChE.
Please forward this to your colleagues who may be
interested.
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