TAILIEUCHUNG - Medicines & Medical Devices Regulation: What you need to know

The sequencing of the human genome together with the development and implementation of new high throughput technologies (so called “omics”) are enhancing our knowledge on human health and disease and have already, and will continue, to provide a sound foundation for personalised medicine. The workshop “Omics in personalised medicine” that was held at the European Commission in Brussels on 29th and 30th of April, brought together experts from different fields: omics, epidemiology, pharmacology, experimental medicine and bioinformatics representing academia, industry, including SMEs, and regulatory and funding agencies. The aim of the workshop was to explore the. | Safeguarding public health through the effective regulation of medicines and medical devices Medicines Medical Devices Regulation What is the MHRA 2 When is a product acceptably safe 2 The history of UK regulation 3 How does the MHRA work 4 How does licensing and authorisation work 5 How is a medicine licensed 5 Monitoring new medicines and vaccines 6 How are devices authorised 7 What the MHRA licenses authorises 7 Herbal medicines and homeopathic remedies 8 Why are clinical trials important 9 How does the MHRA monitor safety and 10 quality standards Safety and quality standards 10 Why is the General Practice Research 11 Database important A patient s view of the Yellow Card Scheme 12 What happens when quality or safety 13 concerns arise Dealing with faulty medicines 14 Responding to concerns about devices 16 How device reporting makes a difference 17 Is it safe to order medicines and devices off 18 the internet Influencing Policy 19 Medicines Medical Devices Regulation

• Y học thường thức
• human genome
• human health and disease
• Pancreatic Lesion
• Coagulation Disorders
• Clinical Implications
• Expandable Metallic
• Genome Biology
• Ashkenazi human
• Human reference genome
• Single reference genome
• Population specific reference genomes
• Regulatory elements
• Non coding regions
• Genome wide quantification
• Endogenous functionality
• Pan genome
• Core genome
• Presence absence variation
• Genome assembly
• Population specific variation
• Splice site
• Protein variant
• Molecular evolution
• SMOX gene exon
• BMC Genomics
• Genomic variation
• Alternate alleles
• Potential functional significance
• Horizontal gene transfer
• Eukaryotic genomes
• Phylogenetic trees
• Machine learning
• Semi automated genome annotation methods
• Genome wide measurements
• Cell type
• Genetic variation in populations
• Genome analysis
• Introduction to the human genome
• Human genetic diversity
• Genetics in medicine
• The molecular basis of genetic disease
• Identifying the genetic basis for human disease
• Estimated incidence
• Human papillomavirus
• Helicobacter pylori
• Human sequencing reads
• Transcriptional repression
• Genome higherorder organization
• Transcriptional activity
• Genome editing
• Transform human medicine
• Biological consequences
• Beta thalassemia
• Human cells
• Mouse cells
• Single RNA guided endonuclease system
• Genome engineering
• Human population genetics
• Genome diversity
• Whole genome sequences
• Archaic introgression
• Population demography
• Genome scale approaches
• Human disease genomics
• Human genetic research
• Complex neuropsychiatric disorder
• Population genetics
• Human population genetic analysis
• DNA level
• Human evolution
• Post translational modification
• Ubiquitin modulates
• Human proteins
• Human gut microbiome
• Primate gut microbiome
• Highlight microbiome traits
• Biochemistry
• molecular Biology
• biological cells
• genetics
• Scientific reports
• Interpreting the human
• genome sequence
• stochastic grammars
• báo cáo khoa học
• mô hình ngôn ngữ
• xử lý ngôn ngữ tự nhiên
• Human Genome Project
• Gene therapy
• Personalized medicine
• Omic disciplines
• Genomic era
• DNA methylation particularly
• Human genome function
• Genome function
• Human phenotypes
• Epigenome wide association studies
• Non tuberculosis mycobacterium
• Whole genome sequencing
• Non tuberculous mycobacterial pulmonary disease
• Human to human transmission
• Gene regulation
• Genomic imprinting
• ZFBS morph overlaps
• Density plots
• Human embryonic stem cell
• Nanopore sequencing
• Long read sequencing
• Next generation sequencing
• Somatic mutation
• Structural variant
• Biotin capture
• Topologically associating domains
• Hierarchically organized
• RNA polymerase III