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Phases of Clinical Trials

Phases of Clinical Trials

Clinicaltrials are conducted to gather knowledge relating to the security and effectuality of recent drug and device development. There are many steps andstages of approval within the clinical trials method before a drug or device may be sold within the client market

Phase I studies assess the security of a drug or device.

Phase II studies check the effectuality of a drug or device.

Phase III studies involve randomized and blind testing in many hundred to many thousand patients.

Phase IV studies, usually known as Post marketing Trials, are conducted once a drug or device has been approved for client sale.

Related:  Clinical Trials ConferencesClinical TrialConferences | Pharmacovigilance  Conferences | Clinical Trials Congress |ClinicalTrials Meetings | MedicalConferences | PharmacologyConferences | ClinicalResearch Conferences | Clinical research Society | Clinical Research Associations 

Recommended: 9th World Congress on Clinical Pharmacyand Pharmacy Practice Amsterdam, Netherlands March 25-26, 2019, 4thInternational Conference onMedical Microbiology 2019 Vienna, Austria May 20-21, 2019, CPD Accredited8th European ClinicalMicrobiology and ImmunologyCongress Edinburgh, Scotland June 12-13, 2019, International Conference on Clinical TrialsPharmacovigilance,Prague Czech Republic, September 26 -27 2019. World Congress on Biomarkers andClinical Research, Tokyo, Japan, August 5-6, 2019.

Related AssociationsThePharmaceutical Society of Australia (PSA), AustrianPharmaceutical Society (APS), KoreanResearch-based Pharmaceutical Industry Association (KRPIA), KuwaitPharmaceutical Association (KPA), IndianPharmaceutical Association (IPA).

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