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PHARMACEUTICAL LIBRARY

CV

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Curriculum Vitae (CV) A summary of a job applicant’s professional experience and educational background, along with other relevant information regarding the candidate’s qualifications. The curriculum vitae is similar to a resume, but is used more frequently by candidates who have published works in journals, such as scientists or academic professionals.The CV usually is requested with […]

R&D

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Research and Development (R&D) Research and development (R&D) refers to the investigative activities a business conducts to improve existing products and procedures or to lead to the development of new products and procedures.

SOPs

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Standard Operating Procedures (SOPs) A standard operating procedure, or SOP, is a set of step-by-step instructions compiled by an organization to help workers carry out routine operations. SOPs aim to achieve efficiency, quality output and uniformity of performance, while reducing miscommunication and failure to comply with industry regulations.

GCP

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Good Clinical Practice (GCP) The tripartite harmonised ICH Guideline was finalised under Step 4 in May 1996. This Good Clinical Practices document describes the responsibilities and expectations of all participants in the conduct of clinical trials, including investigators, monitors, sponsors and IRBs. GCPs cover aspects of monitoring, reporting and archiving of clinical trials and incorporating […]

EU

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European Union (EU) The European Union is a unique economic and political union between 28 European countries that together cover much of the continent. The EU was created in the aftermath of the Second World War. The first steps were to foster economic cooperation: the idea being that countries that trade with one another become […]

ICH

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International Council for Harmonization (ICH) The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has the aim of bringing together the regulatory authorities and pharmaceutical industry to discuss scientific and technical aspects of drug registration. Since its inception in 1990, ICH has gradually evolved, to respond to the increasingly global […]

EMA

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European Medicines Agency (EMA) Once known as the European Medicines Evaluation Agency (EMEA), the European Medicines Agency (EMA) is a decentralised agency of the European Union (EU), located in London. It began operating in 1995. The Agency is responsible for the scientific evaluation, supervision and safety monitoring of medicines in the EU. For further details […]

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