medical report

When the liaison agency of one Party must submit the existing medical report for the purposes of deciding on a claim or changing the benefit of the other Party, this report must be provided and submitted to the other Party as soon as possible.

If the Competent Institution of one Party requires the claimant or beneficiary permanently residing in the territory of the other Party to undergo a medical examination, the liaison agency of the latter Party will at the request of the liaison agency of the former Party, make the arrangements for a medical examination in accordance with the rules applied by the liaison agency making the arrangements at the expense of the liaison agency requesting the medical examination and will provide the medical report of the examination in a mutually determined form.

In the case of a claim for a benefit that depends on a person` s disability, the Competent Institution of the Party in whose territory the person permanently resides will provide a medical report under Article 6 of the Agreement at the request of the other Competent Institution.

In his contribution the author reports on the activities of the Republic Expert Committee for Medical Ethics.

The previous and existent legislation study, published reports on health reforms objectives and enfficiency, medical, sociological and economic proceedings are the basis of a qualitative social medical analysis of conditions which influence on the physician present and future work.

The 2004 report from the United Kingdom` s Chief Medical Officer on the impact of physical activity and its relationship to health estimated the cost of physical inactivity at GBP 8.2 billion annually (including both the health care cost and the wider cost to the economy, such as days lost from work) fn.

To assist in the assessment referred to in paragraph 1, the Competent Institution of the Party in whose territory the person resides shall, at the request of the Competent Institution of the other Party forward to the latter free of charge any existing relevant medical reports and documents that it has available.

The AACC may, after obtaining the advice of a medical officer authorised by the Agency, decide that the one month time limit within which the application must be made and the six month limit provided for in the paragraph 2 shall not apply where the person concerned is suffering from a serious or protracted illness contracted during his employment, which he has reported to the Agency before the end of the six month period provided for in the paragraph 2, on condition that the person concerned undergoes a medical examination arranged by the Agency.

Medical reports usually come from large airports such as Tokyo, London and Paris.

A report on firecrackers comes with a photo of a mangled hand, the kind of image that once used to be limited to forensic medical textbooks.

In contrast to various crime experts, for example, medical staff, criminologists, prosecutors and judges, reporters do not come into close contact with violence.

Acting in accordance with the guidelines, marketing authorisation holders shall use internationally agreed medical terminology for the reporting of adverse reactions.

THE STAFF MEMBER MAY SUBMIT TO THE INVALIDITY COMMITTEE ANY REPORTS OR CERTIFICATES FROM HIS REGULAR DOCTOR OR FROM ANY MEDICAL PRACTITIONERS WHOM HE MAY HAVE CONSULTED.

In accordance with this guide, holders of marketing authorisations shall use the medical terminology accepted at international level for the transmission of adverse-reaction reports.

in Article 77(1), the second subparagraph shall be replaced by the following:"In accordance with those guidelines, the marketing authorisation holder shall use internationally agreed veterinary medical terminology for the transmission of reports on adverse reactions.

However, in the case of those Member States not requiring annual medical check-ups on the date of adoption of this Directive, pursuant to existing veterinary laws, the medical check-up provided for in Annex A, Chapter II (17), shall be obligatory only from 15 February 1980, unless the Council, acting on a proposal by the Commission, decides before 31 December 1979 to postpone that date in the light of the report which the Commission will submit to it.

Stereotyping, medicalization, sexualization, the veil of secrecy and, after all, normalization too (e.g. they are just like us but not quite) are those areas within media representations where reporting breaks loose from the harnesses of political correctness and steps over the edge.

Determination of the degree of invalidity In order to determine the degree of invalidity, the institution of the Member State shall take into consideration the documents and medical reports and the information of an administrative nature obtained by the institution of any other Member State.

forward, without delay, to the institution of the Member State under whose legislation the person suffering from the disease previously pursued an activity which might cause the disease in question, the notification and all accompanying documents, including the findings and reports of the medical examinations arranged by the first institution, and a copy of the decision referred to under (b);

The recommendations of the Scientific Committee as well as further information by the notifier were taken into account during the further review and in this Directive and in the Review Report, where the need for monitoring of operators and worker based on medical surveillance to detect negative effects without delay as well as monitoring studies to quantify DDR contamination under practical conditions is stressed.

First, it placed homosexuality in the field of the secret and the alien, which, by the way, was a typical approach in media reporting throughout the thirty years analyzed here. Second, it medicalized the issue of homosexuality, much like all other six textsabout this issue that appeared in the 1970s. In these texts homosexuality was addressed through medical or psychiatric discourse, partly also criminal discourse, and referred to as a 'mistake,' 'a mistake of nature,' 'genetic mistake,' and so on.

In order to facilitate the exchange of information on pharmacovigilance within the Community, the Commission, after consulting the Agency, the Member States and interested parties, shall draw up guidelines on the collection, verification and presentation of adverse reaction reports, including technical requirements for electronic exchange of pharmacovigilance information in accordance with internationally agreed formats, and shall publish a reference to an internationally agreed medical terminology.

This report shall indicate in particular the nature of the employment, the amount of earnings or means which the person concerned has had during the last complete quarter, the normal remuneration paid in the same area to a worker at the same level as the person concerned in the occupation which he followed before becoming an invalid over a reference period to be determined by the institution responsible for payment and, where appropriate, the opinion of a medical expert on the state of health of the person concerned.

The contracting authority may request the consultant and/or his personnel performing the services to undergo a medical examination by a qualified medical practitioner before leaving his or their usual place of residence and shall as soon as is practicable furnish the contracting authority with the medical report resulting therefrom.

is true both with respect to reports by, for example, health care providers, to pharmaceutical and medical device companies, and with respect to reports by pharmaceutical and medical device companies to government agencies like the Food and Drug Administration.

Also, FCRA prohibits credit reporting agencies from providing medical information for employment purposes without the consent of the consumer.

The written report, signed by the medical practitioner or other authorized person responsible, must contain a critical evaluation of all the data collected during the clinical investigation.

c) Marketing authorisation holders must arrange for essential clinical trial documents (including case report forms) other than subject's medical files, to be kept by the owners of the data:

Does a pharmaceutical or medical device firm have to apply the Safe Harbor Principles with respect to notice, choice, onward transfer, and access in its product safety and efficacy monitoring activities, including the reporting of adverse events and the tracking of patients/subjects using certain medicines or medical devices (e. g. a pacemaker)?

The undersigned declares that during his term of employment he will immediately report to the management and the medical service of the undertaking or to his family doctor any contagious disease from which he is or thinks he is suffering.

In order to determine the degree of invalidity, the institution of the Member State shall take into consideration the documents and medical reports and the information of an administrative nature obtained by the institution of any other Member State.

Areas where the states have taken action include bank records, cable television subscriptions, credit reports, employment records, government records, genetic information and medical records, insurance records, school records, electronic communications, and video rentals (I2).

the establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the company and to medical representatives, is collected, evaluated and collated so that it may be accessed at a single point within the Community;

At the end of the treatment, a detailed report shall be forwarded to the competent institution together with medical certificates concerning the permanent consequences of the accident or disease, and in particular the present condition of the victim, and the recovery from the injuries or their consolidation.

This report shall indicate in particular the nature of the employment, the amount of earnings or means which the person concerned has had during the last com-plete quarter, the normal remuneration paid in the same area to a worker at the same level as the person concerned in the occupation which he followed before becoming an invalid over a reference period to be determined by the institution responsible for payment and, where appropriate, the opinion of a medical expert on the state of health of the person concerned.

Within three years of the entry into force of this Regulation the Commission shall produce a report on whether the level of harmonization achieved by this Regulation and by Council Directive 90/167/EEC of 26 March 1990 laying down the conditions governing the preparation, placing on the market and use of medicated feedingstuffs in the Community (2) is equivalent to that provided for in Council Directive 70/524/EEC, accompanied if necessary by the proposals to modify the status of the coccidiostats and other medicinal substances covered by that Directive.

The importance to report medication errors, and their causes and consequences.

Medically important adverse reactions reported at an incidence greater than placebo in controlled clinical studies and medically important adverse reactions reported through post- marketing surveillance

Reports shall include statements on incidents, and coercive and medical measures, if any have taken place.

The response document included a review of clinical data (published data, medical research reports) and microbiological data.

In its Report on specific training in general medical practice provided for by Title IV of Directive 93/16/EEC, the Commission recommended that the requirements applying to part-time training in general medical practice should be brought into line with those applying to other medical specialists.

This is true both with respect to reports by, for example, health care providers, to pharmaceutical and medical device companies, and with respect to reports by pharmaceutical and medical device companies to government agencies like the Food and Drug Administration.

In the clinical studies, subjects in the Safety Population reported any new medical conditions during the follow-up of up to 4 years.

In addition, the frequency of medically important adverse reactions reported from post-marketing experience is included as not known.