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Seminar on Medical Ethics, presented on 11/02/2018
Regulatory writing
here are the clinical research terminologys
Regulatory Affairs
Basics terminologies constantly used in computerized system validation . This is an initiative for a...
Drug development , uses and it's applications, pre clinical trails
Working on Clinical Trials – Getting started Very few clinical trials are conducted only in one c...
Informed Consent Form is an form where subject voluntarily shows his / her willingness to participat...
Japan Regulation Drug Regulatory Affairs
ensayos farmacovigilancia
This presentation comprises information about clinical trial supply management.
Stability, safety, advertising , labelling and packaging of biologics in EU
Organization and objectives of ICH, expedited reporting, ICSR, PSURs, post approval expedited report...
Contract Research Organisations- An Overview in Pharma Field
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
Crp
A presentation on INFORMED CONSENT FORM which is easy to understand and easy to explain and in very...
The safety monitoring in a clinical trail accompanies by common practices in safety monitoring, comm...
An informed consent form is a document that is provided to prospective participants in a research st...
Requirements And Guidelines For Permission To Import / or Manufacture of New Drugs For Sale or To Un...
quality control tools, NABL, ISO 9000, ISO 14000 , total quality management, quality by design, ICH ...
quality audit of pharamceutical documentation
Safety Monitoring in Clinical Trails, Safety Proicedures to be Fallowed
