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  2. Pharmaceutical Inspection Convention and Pharmaceutical ...

    en.wikipedia.org/wiki/Pharmaceutical_Inspection...

    The PIC (Pharmaceutical Inspection Convention) was founded in October 1970 by the European Free Trade Association (EFTA), under the title of the Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products. [1] [2] The initial members comprised the 10 member countries of EFTA at that time.

  3. Pharmacy management system - Wikipedia

    en.wikipedia.org/wiki/Pharmacy_management_system

    The pharmacy management system serves many purposes, including the safe and effective dispensing of pharmaceutical drugs. During the dispensing process, the system will prompt the pharmacist to verify the medication they have is for the correct patient and has the correct quantity, dosage, and information on the prescription label.

  4. Clinical data management system - Wikipedia

    en.wikipedia.org/wiki/Clinical_data_management...

    A clinical data management system or CDMS is a tool used in clinical research to manage the data of a clinical trial. The clinical trial data gathered at the investigator site in the case report form are stored in the CDMS. To reduce the possibility of errors due to human entry, the systems employ various means to verify the data.

  5. Clinical trial management system - Wikipedia

    en.wikipedia.org/wiki/Clinical_trial_management...

    A Clinical Trial Management System (CTMS) is a software system used by biotechnology and pharmaceutical industries to manage clinical trials in clinical research. The system maintains and manages planning, performing and reporting functions, along with participant contact information, tracking deadlines and milestones.

  6. Process analytical technology - Wikipedia

    en.wikipedia.org/wiki/Process_analytical_technology

    With this framework – according to Hinz [2] – the FDA tries to motivate the pharmaceutical industry to improve the production process. Because of the tight regulatory requirements and the long development time for a new drug, the production technology is "frozen" at the time of conducting phase-2 clinical trials.

  7. Contract manufacturing organization - Wikipedia

    en.wikipedia.org/wiki/Contract_manufacturing...

    A contract manufacturing organization (CMO), more recently referred to (and more commonly used now) as a contract development and manufacturing organization (CDMO) to avoid the acronym confusion of Chief Medical Officer or Clinical Monitoring Organization in the pharma industry, is a company that serves other companies in the pharmaceutical industry on a contract basis to provide comprehensive ...

  8. Subsidy Scorecards: Ohio State University-Main Campus

    projects.huffingtonpost.com/projects/ncaa/...

    SOURCE: Integrated Postsecondary Education Data System, Ohio State University-Main Campus (2014, 2013, 2012, 2011, 2010).Read our methodology here.. HuffPost and The Chronicle examined 201 public D-I schools from 2010-2014.

  9. Pharmacoinformatics - Wikipedia

    en.wikipedia.org/wiki/Pharmacoinformatics

    The first dedicated department for Pharmacoinformatics was established at the National Institute Of Pharmaceutical Education And Research, S.A.S. Nagar, India in 2003. [2] This has been followed by different universities worldwide including a program by European universities named the European Pharmacoinformatics Initiative (Europin [ 3 ] ).