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Media Statement Successful Launch to the IMDRF
Origin/Publisher:
IMDRF
Content:
Good progress and a commitment to advancing regulatory convergence and public health marked the inaugural meeting of the International Medical Device Regulators Forum (IMDRF), held in Singapore from 28 February to 1 March 2012. Regulators from Australia, Brazil, Canada, Europe, Japan, and the United States of America were joined by regulatory observers from China and the Russian Federation and by the World Health Organization for the purpose of putting the new Forum into operation and planning the transition of several key items from the Global Harmonization Task Force.
GMP Conferences by Topics
- General Quality Assurance and GMP Compliance Topics
- Hygiene
- General Microbiology Topics
- Regulatory Affairs
- Development
- General Analytics Topics
- Good Distribution Practice
- Sterile Manufacturing
- Computer Validation
- General Qualification/Validation Topics
- General Engineering Topics
- APIs/Excipients
- GMP Basic Training Courses
- Medical Devices and Combination Products
- Packaging and Packaging Material
- Data Integrity
- Qualified Person (QP)
- GMP Auditing
- Documentation
- Cleaning Validation
- General IT Compliance Topics
- Impurities
- OOS / OOE / OOT
- Material Testing
- Validation of Analytical Methods
- Analytical Instrument Qualification
- Stability Testing
- Microbiological Testing
- Technology
- General Manufacturing Topics
- Solid Dosage Forms/Semi-Solid Dosage Forms
- Biotechnology/Blood/ATMP
- Herbal Drug Products/Cannabis/Radiopharmaceuticals
- Others