The
Cleanroom Management
Summit would like to highlight Annex 1 compliance, audit
readiness and isolator technology as the essential topics for the
pharmaceutical and healthcare industries. Included in the Summit’s Agenda they
will result in overall industry development and shall help generate better
understanding and expertise.
Annex
1, is an important industry requirement which requires compliance for sterile
manufacturing of medicinal products. This standard is being revised in coming
months, it is important that we understand the changes and how they would
affect the manufacturing process. The Summit will highlight the new changes and
our industry expert Mr Farguharson will provide guidance on how to maintain
compliance.
Audits
are very important in the drug manufacturing industry, they ensure the high
quality standards, operational safety & efficiency and the regulatory
requirements are achieved to ensure the safety of the customers, therefore
preparation for auditing is essential, the Summit will look at this topic in
detail with our industry leader giving insight and guidance on how to be Audit
ready and how to achieve GMP excellence, these topics will provide essential
information and would help your next industry audit go smoothly and incident
free.
Isolator technology
provides an easier and more cost effective solution for the cleanroom industry,
the Summit will see how this technology can be implemented in pharmaceutical
manufacturing and it's impact on the overall cleanroom industry.
Special book offer:
Posted by Dr. Tim Sandle
