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RESPONSIBILITIES FOR MONITORING

Autonomic nervous system. The portion of the nervous system outside of the brain and spinal cord that is responsible for monitoring and controlling the digestive system, cardiovascular system, and other organs that are not under direct conscious control. [Pg.450]

Inform the patient about the potential drug-drug interactions with warfarin, including over-the-counter medications and dietary supplements (Tables 7-8, 7-9, and 7-10). Instruct the patient to call the health care practitioner responsible for monitoring warfarin therapy before starting any new medications or dietary supplements. [Pg.158]

The cytosol is the fluid compartment of the cell and contains the enzymes responsible for cellular metabolism together with free ribosomes concerned with local protein synthesis. In addition to these structures which are common to all cell types, the neuron also contains specific organelles which are unique to the nervous system. For example, the neuronal skeleton is responsible for monitoring the shape of the neuron. This is composed of several fibrous proteins that strengthen the axonal process and provide a structure for the location of specific membrane proteins. The axonal cytoskeleton has been divided into the internal cytoskeleton, which consists of microtubules linked to filaments along the length of the axon, which provides a track for the movement of vesicular material by fast axonal transport, and the cortical cytoskeleton. [Pg.10]

Effective handling of all information relating to drug safety is one of the most important responsibilities, if not the most important responsibility, of the medical department. The size of a company and the volume of work will dictate whether the responsibility for monitoring drug safety resides with members of staff who have... [Pg.337]

The IRB is responsible for judging all studies to be conducted at the centre concerned by reviewing protocols, the informed consent sheet, the investigator s brochure and other materials relating to the conduct of clinical trials. The IRB is also responsible for monitoring whether the clinical trials are conducted in compliance with both GCP and IRB s requirements, if any. When the study period of a clinical trial exceeds 1 year the IRB should review the study every year. As the new GCP allows the study sponsor to pay a reasonable amount of money to the study subjects, the IRB is expected to review whether the amount and method of payment is reasonable and does not infringe upon the ethical aspects of the study. Also, the advertisement of a trial for patient recruitment is allowed, but the IRB s approval to implement this at the study centre is required. [Pg.645]

Governmental drug-regulating agencies have responsibility for monitoring drug safety. In the USA, the FDA-sponsored... [Pg.1378]

The Texas Air Control Board was responsible for monitoring emissions of hydrogen sulfide and sulfur dioxide during all phases of the Sulphlex construction The measurements indicated that neither gas was present at levels near those which would pose a safety or environmental hazard during any phase of the operation. [Pg.221]

For a pharmaceutical firm, the name of the person responsible for monitoring the conduct of the clinical investigation and reviewing and evaluating safety information should be entered. For Sponsor-Investigator INDs, the investigator has this responsibility. [Pg.100]

An important question in this area relates to the widespread use of exposure biomarker responses for monitoring effluents and receiving waters for endocrine disrupter activity. In oviparous species, vitellogenin is the major example of such a... [Pg.84]

NAME AND TITLE OF THE PERSON RESPONSIBLE FOR MONITORING THE CONDUCT AND PROGRESS OF THE CUNICAL INVESTIGATIONS... [Pg.70]

Descriptive title of the nonclinical research study Purpose of conducting the study Where and by whom the study is to be conducted Company that is sponsoring the study Sponsor s agent who is responsible for monitoring the study CRO senior staff who will be responsible for the various aspects of the study... [Pg.446]

The Quality Assurance organization has no mandated role in the development of computer systems other than defining QA fnnctional reqnirements. Once the system has been validated, accepted, and installed, QA will be responsible for monitoring data collection until its reliability is confirmed in accordance with SOP, compliance of nser SOPs, training, and secnrity policies. Any performance problems shonld be commnnicated to the responsible management persotmel in a timely fashion. QA shonld monitor corrective actions and nnschednled downtime records. [Pg.544]

The simplest color sensing systems are responsible for monitoring only one color across a scene. These are typically used in quality control applications such as monitoring of paints, to ensure consistency between batches made at different times. More sophisticated color sensors look at the color distribution across a two-dimensional image. These systems are capable of complex analysis and can be used for checking multi-colored labels or for identifying multi-colored objects by their color patterns. [Pg.185]


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Responsibility for

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