Administration and supervision

Organization, administration, and supervision of safety activities in accordance with all federal, state, and local requirements... 

Hutson, 1923. P. W. Hutson. High-School Science Teachers A Study of Their Training in Relation to the Subjects They Are Teaching . Educational Administration and Supervision 9 423 438. 

Review by supervisory body Dmg regulatory legislation normally specifies the official chain of command and the supervisory body to which the DRA must report. Administrative and legislative supervision is an important means of accountability if properly applied. However, supervision should not be used as a means of political influence over legitimate regulatory decisions. 

The number and size of daily doses, time of administration, and diet and exercise require continuous medical supervision. Dosage adjustment may be necessary when changing types of insulin. Rotate administration sites to prevent lipodystrophy. Do not administer within 1 inch of the same site for 1 month. It may be best to rotate sites within an area rather than rotating areas. 

Self-administration Etanercept is intended for use under the guidance and supervision of a physician. Patients may self-inject only if the physician determines that it is appropriate and medical follow-up is provided, as necessary, after proper training in injection technique and how to measure the correct dose. 

Although the safety profile of SLIT is satisfactory, it is important to underline that physicians who prescribe IT need adequate training in allergology and specialist supervision is always necessary. The therapy should only be prescribed by specialists, after a detailed diagnosis has been made and the expected benefit/cost ratio has been carefully evaluated. Patients should be instructed to carefully follow the manufacturer s schedule of administration and to visit the clinic at least every 3 months. Only standardized extracts with proven efficacy (grass, Parietaria, mites, olive, birch) should be used. Since SLIT (and LNIT) is self-administered, detailed instructions and follow-up of the patients are mandatory. 

Kochetkov s duties included the administration and scientific supervision of the Institute. In line with the Academy of Sciences practice for directors, he chaired the IOKh s Scientific Council. In one of his last interviews, Nikolay said he thought it would be tragedy for a scientist to become just the manager of an enterprise, and he was able to avoid that. He remained a devoted scientist, while becoming an excellent manager and administrator. He maintained traditions that had developed since the Institute was founded in 1934. 

Although the board delegates day-to-day financial matters to the CEO, it is impossible for one person to supervise all aspects of the hospital s operations. The number of internal and external demands that require the CEO s personal attention and the highly technical nature of operations require the CEO to delegate many tasks to the hospital s senior managers and department directors. Indeed, financial management is a principal function of all administrators and managers. 

Director. The Director is a professional woman archivist who reports to the Director General of Archives and Libraries. She is responsible for the supervision of the Center in all respects scientific, technical, administrative, and training. Coincidentally, she has a second and correlated responsibility Director, National Center for Microfilm. 

A Commission secretariat (in DG Sanco) runs administration and helps coordinate and supervise the three scientific committees. This secretariat has an important function as a link between the scientists and the Commission. The secretariat is also a point of contact for external stakeholders. In addition, an inter-committee coordination group has been set up in order to manage overlapping issues and to avoid contradictory advice. 

The Agency is a corporate body with perpetual succession and a common seal and may sue and be sued in its corporate name. It has an established council with a chairman appointed by the President, Commander-in-Chief of the Armed Forces on the recommendation of Minister of Health. The Director-General of the Agency is the Chief Executive Officer who will be responsible for the day-to-day administration and will keep the books and records of the Agency. He shall, however, be subject to the supervision and control of the chairman and council. 

Compliance with medication/device use (by the study subject) should be assessed in all studies. If supplies are dispensed to subjects for selfadministration, methods to assure compliance (e.g. diary cards, instructions on labeling, supervised administration) and methods to check compliance (e.g. tablet counts, plasma/urine assays, diary card review) must be in place. At each study visit, the study subjects should be asked to... 

Since 1993, there is an administrative authority responsible for medicines in the entire European Union, enacted by Council Regulation (EEC) No. 2309/93. This European Agency for the Evaluation of Medicinal Products (EMEA) is responsible for coordinating the scientific resources put at its disposal by the competent authorities of the member states for the evaluation and supervision of medicinal products for human use. A marketing authorization granted under the centralized procedure by EMEA is valid for all member states. 

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