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The European Compliance Academy (ECA) announced today that it appointed Dr
Robert Johnson as Chairman of its Working Group for Rapid Microbiological
Methods (RMM). He follows Mike Edgington in this position, who deceased in
January 2007.
Dr Johnson has already been member of the RMM Working Group
since its foundation in June 2006. He holds a Bachelor in Biology and a
Ph.D. in Microbiology. He is also a registered Qualified Person as well as
member of various professional bodies such as the Institute of Biology and
the American Society of Microbiologists. "I'm honoured by the appointment
and I look forward to working with the group to support both authorities and
industry in getting a better understanding of the requirements and thereby
advancing the introduction of RMMs," Dr Johnson said.
"With more than 25 years in leading positions in the
industry, Dr Johnson brings a wealth of practical experience to ECA", said
Daniel Scheidegger, ECA Chairman and Vice President Operations and Managing
Director of Genzyme Pharmaceuticals, Liestal, Switzerland. "We're very
grateful that he accepted our invitation to lead the Working Group", he
continued.
About the Working Group Rapid Microbiological Methods
(RMM)
The Working Group was founded in June 2006. Its goal is to
maintain the European pharmaceutical industries competitive position through
providing both regulatory agencies and the industry with sufficient
information on new technologies that will allow them a rapid and simplified
decision making process and thus increase drug safety and reduce cost. To
accomplish its goal, the group is presently working on establishing a best
practice guide to reflect current practice and thinking. To find out more
about the group please read here.
About the ECA
Founded as an independent organization in 1999, the
European Compliance Academy's (ECA) goal is to facilitate the move towards a
harmonized set of GMP and regulatory guidelines. It supports the
Pharmaceutical Industry and Regulators through providing information on and
interpretation of new or updated guidances. For that purpose the ECA
developed a range of tools like the GMP Guideline Manager CD-ROM, and also
organizes international education courses, webinars and conferences around
GMP, regulatory compliance and currently discussed subjects. For further
information on the ECA please refer to
www.gmp-compliance.org.
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