ECA Validation Group: Survey Results
The ECA Validation
Group which currently counts 193 members is one of ECA's seven Working/
Interest Groups. We've asked the members of the Validation Group about their
topics of interest and in which direction the group should evolve.
In total, 84
participants answered the survey. Yet, not every question has been answered to
by all the participants. 72.5% of the respondents work for international
companies, 17.5% in national companies and 10% have a field of activity in
Europe. For 68%, the centre of interest strongly focuses on the EU, 38% are
particularly interested in the FDA.
Half of the responses came from companies
with less than 100 employees, 29.7% of the responses came from persons who work
in companies with up to 500 employees and 20.3% of the participants work at
large companies (> 500 employees).
The production range of the companies at
which the participants are employed mainly concerns finished products (59%),
and then biologics with 19.2%, and 11.5% manufacture APIs. Another 10.3% are
employed in distribution. Regarding the horizon of experience, the participants
are mainly highly experienced. 68.3% of them have more than 3 years of
practical experience in their current field of activity. No fewer than 20.7%
have close to 3 years experience and 11% of the respondents have been already
working for at least one year. For the majority (43%), Qualification/Validation
is one activity amongst others. 27.8% of the participants occupy 50% of their
daily working time with the topic Qualification/Validation and 29.1% operate
Validation/Qualification more than 50% of their daily working time.
Now, about the
survey itself. The interest frontrunner is Process Validation, followed by
Cleaning Validation and Requalification on third place. It is interesting to note
a still high medium interest for the qualification of delivery systems (see
illustration 1).
Illustration 1 -
Overview of the ECA Validation Group members' centres of interest, as of July
2016
Only a few further comments have been made. An accumulation of
topics couldn't be observed in the comments. Only the topic Computer Validation
was mentioned twice. Yet, ECA has an own IT Compliance Group.
Apart from that, the following topics were named: On-going Process
Verification, Cleaning Validation in "shared facilities", Change
Control during Qualification/Commissioning, Lean Qualification, Data Integrity
factors, Equipment Qualification vs. Computer Validation, Risk Analysis,
Periodic Review of the validation status, validation level at suppliers.
In the survey, the question was also asked in which direction the
group should evolve (Business Plan). Here again, there was no clearly similar
answers. Two participants wish current GMP-related topics, whereby one of the
answers stated "what the ECA already offers". Besides, the following
preferred topics were mentioned: Statistical Evaluations, Sample Plans,
Knowledge Management, Cleaning Validation for the manufacture of veterinary
medicinal products, Assessment of the current Developments in industrial
Process Validation (classical validation vs. hybrid vs. continuous),
Interaction between On-going Process Verification and PQR, Process Validation in
the area of biologics, Modern Cleaning Validation.
Conclusion
For the ECA Validation Group members who participated in the survey, their centres of interest are: Process Validation, Cleaning Validation and Requalification. Particularly interesting are (also) future current GMP topics in the area Validation/Qualification.
For the ECA Validation Group members who participated in the survey, their centres of interest are: Process Validation, Cleaning Validation and Requalification. Particularly interesting are (also) future current GMP topics in the area Validation/Qualification.
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