GMP Compliance requires informed Staff in the Lab

The increasing attention authorities devote to the quality management and laboratory compliance emphasise the importance of the work in the laboratory for pharmaceutical development and manufacturing. That's why responsible staff has to focus even more on the establishment of GLP and GMP standards in deployed systems and methods. To analyse and process the multitude of accumulated results and data GMP compliantly and to ensure the validity of systems such as LIMS pose additional challenges.

For laboratory staff it is difficult to stay on top of these developments. Frequently, courses or conferences are only suitable to a limited extent to convey knowledge and current trends. The same is true for laboratory equipment fairs. For visitors and exhibitors with a focus on “Pharma” they are too unspecific and too big. For specialised exhibitors, this means many visitors, but little professional exchanges on the other side.

Therefore, PharmaLab will start in 2013. This new laboratory Congress’ goal is to provide lab employees in the pharmaceutical industry with current knowledge relative to developments, applications and validation in analytics, bioanalytics and microbiology. It also aims at facilitating the exchange of information and experience with regard to GMP compliance in laboratories.

In six conferences 40 speakers from industry, contract laboratories and from authorities will report about regulatory changes, hands-on experience in the lab as well as about the implementation and validation of methods.

The Congress’ parallel large exhibition which will be located centrally between the conference rooms will also contribute to the information exchange. There, nearly 40 specialised providers will present latest systems and methods as well as services and therefore allow the comparison of available equipment.

PharmaLab 2013
13th/14th November 2013
Swissôtel Düsseldorf
www.pharmalab-Congress.com