We provide information according to our objectives in the fields of

MEDICINAL PRODUCTS

ZLG is central coordination unit of the Laender regarding medicinal products for human and animal use.

• Control of medicinal products in Germany
  • description of the drug surveillance system
  • competent authorities 
  • legal provisions
  • quality assurance in drug monitoring and testing by authorities
  • Committees of the Supreme Laender Authorities and results

• International collaboration regarding the control of medicinal products between the
  • EU Member States and EU institutions
  • the EU and the candidates for accession
  • the EU and third countries

and

MEDICAL DEVICES

ZLG is notifying authority.
 

• accreditation conditions and procedures for 
  • laboratories
  • certification bodies for medical devices and in-vitro-diagnostic
  • certification bodies for quality management systems
  • certification bodies for personnel
  • conformity assessment bodies carrying out assessments according to third counties' legislation (USA, Canadas, Australia and New Zealand)

• Sectoral Committees and information exchange of accredited bodies and laboratories
• Competent authorities (national and international)

besides other interesting topics in related areas.

We are looking forward to meeting you!
 

Dr. Rainer Edelhäuser

Director of ZLG