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Clinical Research Physician Life as a Drug Safety Physician INPHARM.com By Dr Madhu Davies A career in drug safety has the potential to offer a very broad ranging view of the pharmaceutical...
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CRA
Clinical Research Associate:
CRO
Clinical Research Orginization (CRO)
GCP
Good Clinical Practise From Wikipedia, the free encyclopedia good_clinical_practice Good clinical practice is a set of rules and regulations that is provided by International Conference on...
Getting Started in Clinical Research INPHARM.com By Mark Turkish, ETAD Limited The aim of this article is to provide some guidance to fresh graduates, nurses, pharmacists, laboratory staff and...
History of Clinical Trials
If you are allowed to edit pages in this Site, simply click on edit button at the bottom of the page. This will open an editor with a toolbar pallette with options. To create a link to a new page,...
IB
Investigator Brochure 7. INVESTIGATOR’S BROCHURE 7.1 Introduction The Investigator's Brochure (IB) is a compilation of the clinical and nonclinical data on the investigational product(s) that are...
Industry Info INPHARM: Pharmaceutical Jobs and Information
e-CRF Clincal Trial Feasibility and Setup Clinical Trial Management System Clinical Tools
Principal and sub-Investigator in a Clinical Trial 4. INVESTIGATOR 4.1 Investigator's Qualifications and Agreements 4.1.1 The investigator(s) should be qualified by education, training, and...
Job Sites INPHARM: Pharma Jobs
Who can join? Anyone who is currently working in the Pharmaceutical Industry or is interested in Clinical Trials Join! So you want to become a member of this site? Tell us why and apply now! Or,...
Clinical trial From Wikipedia, the free encyclopedia In medicine, a clinical trial (synonyms: clinical studies, research protocols, medical research) is a type of research study. The most commonly...
Pharmaceutical Companies
Pharmacovigilance From Wikipedia, the free encyclopedia Pharmacovigilance the pharmacological science relating to the detection, assessment, understanding and prevention of adverse effects,...
Phase I Phase I trials are the first-stage of testing in human subjects. Normally a small (20-80) group of healthy volunteers will be selected. This phase includes trials designed to assess the...
Phase II Once the initial safety of the therapy has been confirmed in Phase I trials, Phase II trials are performed on larger groups (20-300) and are designed to assess clinical efficacy of the...
Phase III Phase III studies are randomized controlled trials on large patient groups (300–3,000 or more depending upon the condition) and are aimed at being the definitive assessment of the...
Phase IV Phase IV trials involve the post-launch safety surveillance and ongoing technical support of a drug. Phase IV studies may be mandated by regulatory authorities or may be undertaken by the...
Clinical trial protocol From Wikipedia, the free encyclopedia ( clinical_trial_protocol ) A Clinical Trial Protocol is a document that describes the objective(s), design, methodology, statistical...
Recruitment Agencies
Introduction The Uk regulatory invoronment [[cro :cro]] COREC MHRA FDA European Drug Authority
Welcome page Clinical Trials Overview History Phase I Phase II Phase III Phase IV Protocol Design Regulatory and Drug Safety GCP Regulatory Framework Pharmacovigilance Ethical...
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Sponsors of Clinical Trials 5. SPONSOR 5.1 Quality Assurance and Quality Control 5.1.1 The sponsor is responsible for implementing and maintaining quality assurance and quality control systems with...
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Welcome to P. This site is aimed at all the people working in the business end of the pharmaceutical industry from all over the world. The industry is massive so this site is aimed specifically at...
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