Exclusion Criteria. A student can be excluded from the program for any of the following reasons:
1. Student has not been stabilized in an in-patient hospital setting.
2. A less restrictive level of care is available and will be effective.
3. A diagnosis of Mental Retardation and/or cognitive/intellectual limitations only when it would preclude a student’s benefit from the program.
4. Serious Drug or Alcohol dependence/or abuse.
5. Acute suicidal or homicidal ideation/or gestures.
6. A student who is an active sexual perpetrator as evidenced by a recent history of sexually acting out behavior with younger children or a student who is unable to control their sexually acting out behavior/abuse on their own.
7. Student has been accused or adjudicated of a violent crime.
8. A more intensive level of care is required and would be effective.
Exclusion Criteria. Subjects with any of the following characteristics are not eligible to participate in the study:
1. Subjects who were withdrawn from Study BA058-05-003 for any reason.
2. Subjects who experienced a treatment-related SAE during Study BA058-05-003.
Exclusion Criteria. Inclusion and exclusion criteria detailed in the PGD, will be applied to the provision of the service. Patients excluded from the PGD criteria will be provided with information on other local services that will be able to assist them as soon as possible.
Exclusion Criteria. Patients with any of the following characteristics are not eligible to participate in the study.
Exclusion Criteria. 1. The resection of the ileocecal valve is an exclusion criterion because of its association with extensive bowel resection and therefore prolonged parenteral nutrition [10]
2. Colostomy
3. Patients with small bowel atresia are excluded because of prenatally underdeveloped bowel distal to the atresia
4. Multiple ostomies (more than just an enterostomy and a mucous fistula)
5. Patients with chromosomal abnormalities (if known at the time of randomization) are excluded because of potential malabsorption and malnutrition due to an underlying syndrome.
6. Hirschsprung disease secondary exclusion 7. Participation in another drug-intervention study
Exclusion Criteria. Any Bidder is required to confirm in writing that: • Neither it nor any related company to which it regularly subcontracts is insolvent or being wound up, is having its affairs administered by the courts, has entered into an arrangement with creditors, has suspended business activities, is the subject of proceedings concerning those matters, or are in any analogous situation arising from a similar procedure provided for in national legislation or regulations; • Neither it nor a company to which it regularly subcontracts has been convicted of fraud, corruption, involvement in a criminal organisation, any money laundering or terrorism-related offence, any offence concerning professional conduct, breaches of applicable labour law or labour tax legislation or any other illegal activity by a judgment in any court of law whether national or international; • Neither it nor a company to which it regularly subcontracts has failed to comply with its obligations relating to the payment of social security contributions or the payment of taxes in accordance with the legal provisions of the relevant country in which it the Bidder operates. Any Bidder will automatically be excluded from the tender process if it is found that they are guilty of misrepresentation in supplying the required information within their tender bid or fail to supply the required information.
Exclusion Criteria. Tenderers or in case of consortium all members of consortium (as well as all subcontractors) will declare on their honor, by completing and signing Xxxxx X that they are not in any of the situations excluding them from the participation in this tender. The Tenderer which will be selected for the award of the contract shall provide in due time, preceding the signature of the contract, the evidence confirming fulfilment of the Exclusion Criteria, as requested by the contracting authority.
Exclusion Criteria. These describe any conditions that may prevent a patient from receiving treatment within the MAA. These include if a child, young person or adult is diagnosed with an additional progressive life limiting condition where treatment with nusinersen would not provide long- term benefit, such as terminal cancer or catastrophic brain injury. Other exclusions are if the patient/family/carer: • is unwilling to comply with required monitoring criteria that is explained to them • refuses to sign consent to treatment • is unwilling to cooperate with the treatment centre so that they/their child receive the appropriate standard of care management for their condition and circumstances, especially for nutrition and respiratory care and vaccinations, such as influenza and respiratory syncytial virus (RSV).
Exclusion Criteria. Candidates or tenderers shall be excluded from participation in a procurement procedure if:
(a) they are bankrupt or being wound up, are having their affairs administered by the courts, have entered into an arrangement with creditors, have suspended business activities, are the subject of proceedings concerning those matters, or are in any analogous situation arising from a similar procedure provided for in national legislation or regulation
(b) they have been convicted of an offence concerning their professional conduct by a judgment which has the force of res judicata .
(c) they have been guilty of grave professional misconduct proven by any means which the contracting authority can justify;
(d) they have not fulfilled obligations relating to the payment of social security contributions or the payment of taxes in accordance with the legal provisions of the country in which they are established or with those of the country of the contracting authority or those of the country where the contract is to be performed
(e) they have been the subject of a judgment which has the force of res judicata for fraud, corruption, involvement in a criminal organisation or any other illegal activity detrimental to the Communities' financial interest
(f) following another procurement procedure or grant award procedure financed by the Community budget, they have been declared to be in serious breach of contract for failure to comply with their contractual obligations Tenderers must provide a declaration on their honour, duly signed and dated, stating that they are not in one of the situation listed above (see Annex 1). The tender to whom the contract will be awarded must provide evidence confirming the declaration referred to in the previous point. The contracting authority shall accept as satisfactory the following evidence:
i) For points (a), (b) and (e) a recent extract from the judicial record, or failing that, a recent equivalent document issued by a judicial or administrative authority in the country of origin or provenance showing that those requirements are satisfied.
ii) For point (d) a recent certificate issued by the competent authority of the State concerned. Where the document of certificate referred above is not issued in the country concerned and for other cases of exclusion, it may be replaced by a sworn or, failing that, a solemn statement made by the interested party before a judicial or administrative authority, a notary or a qualified professional body in...
Exclusion Criteria. Subjects fulfilling any of the following criteria are not eligible for participation in this study.
1. Any anterior segment infection, inflammation, or abnormality or disease (including systemic) that contraindicates contact lens wear, as determined by the Investigator.
2. Any use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the Investigator.
3. History of ocular or intraocular surgery, including refractive surgery, and/or irregular cornea;
4. Current or previous orthokeratology treatment or has worn rigid gas permeable lenses in the past 12 months.
5. Biomicroscopy findings at screening that are moderate (Grade 3) or higher and/or corneal vascularization that is mild (Grade 2) or higher; presence of corneal infiltrates.
6. Current or history of pathologically dry eye in either eye that, in the opinion of the Investigator, would preclude contact lens wear.
7. Current or history of herpetic keratitis in either eye.
8. Eye injury in either eye within 12 weeks immediately prior to enrollment for this study.
9. Current or history of intolerance, hypersensitivity, or allergy to any component of study lenses, lens care or associated materials for the study.
10. Wearing daily disposable lenses over the last 3 months prior to enrollment.
11. No prior experience with routine cleaning and disinfection.
12. Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment.
13. Any use of habitual/prescribed topical ocular medications or artificial tear or rewetting drops (habitual) that would require instillation during study lens wear.
14. Monovision or multifocal contact lens wearers.
15. The Investigator, his/her staff, family members of the Investigator, family members of the Investigator’s staff, or individuals living in the households of the aforementioned persons may not participate in the study.
16. Participation of the subject in a clinical study within the previous 30 days or currently enrolled in any clinical study.
17. Any habitual wear of Biofinity contact lenses. Women of childbearing potential or women who are pregnant at the time of study entry are not excluded from participation. Pregnancy should be included in the Medical History section of the eCRF when a pregnant woman enters the study or if a woman becomes pregnant during the study. Pregnancy is not reportable as an AE; however, complicatio...
