IMMUNIZATION RECORD Sample Clauses

IMMUNIZATION RECORD. I have provided the childcare operation with a copy of my child’s most current immunization record. ADMISSION REQUIREMENT: If your child does not attend pre-kindergarten or school away from the child-care operation, one of the following must be represented when your child is admitted to the child-care operation or within one week of admission. Please check only one option: 1. HEALTH-CARE PROFESSIONAL’S STATEMENT: I have examined the above named child within the past year and find that he / she is able to take part in the day care program. Health Care Professional’s Signature Date 2. A signed and dated copy of a health care professional’s statement is attached.
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IMMUNIZATION RECORD. Physician Progress Notes Operative Report History and Physical Examination Probation Records Adoption Records Lab, Radiological Reports Physician Orders Medication Records Consultation Records Other: This information is needed for the following purpose(s): Continued Care Other: This authorization is good for one (1) year from the date signed at which it will be null and void. This consent is subject to revocation by the undersigned at any time except to the extent that action has been taken in reliance thereon. I understand revocation must be in writing. Participant DOB: Date Parent/Sponsor (not necessary if Participant is 18 or over) Date AUTHORIZATION FOR OPI TO RELEASE/EXCHANGE INFORMATION I, hereby authorize the Optimum Performance Institute to disclose OPI treatment information and records on to: (Participant Name) PARENT(S)/GUARDIAN/FINANCIAL SPONSOR: OTHER: Name(s): Phone E-mail: Name(s): Phone: E-mail: REFERRAL SOURCE: OTHER: Name: Phone: E-mail: Name(s): Phone: E-mail: OTHER: OTHER: Name: Phone: E-mail: Name(s): Phone: E-mail: The disclosure of this information is for the following purpose: To provide the greatest quality of care by working collaboratively with those who could be of assistance to the participant. This may include weekly updates as to the status and progress of the participant. Information to be released may include (please check): Treatment plan and goals Diagnosis Discharge Planning Progress updates Medication changes Drug/Alcohol test results Behavioral interventions ___ Other _ The transmission of this information my be telephone, mail and or email. OPI will take all precaution regarding electronic transmissions, however, E-mail transmission cannot be guaranteed to be secure or error-free as information could be intercepted, corrupted, lost, destroyed, arrive late or incomplete, or contain viruses. Therefore OPI does not accept liability for email transmissions once it leaves our systems. Limitations of information to be discussed are as follows: Information will not be released by OPI if it is believed that to release it would be harmful or detrimental to the participant’s treatment. I understand that I have a right to receive a copy of this authorization. I understand that any cancellation or modification of this authorization must be in writing and I have a right to revoke it at any time. This authorization shall remain valid for the entire time of receiving treatment at OPI and up to 30 days after discharge. Participant Nam...
IMMUNIZATION RECORD. Please attach a photocopy of your child’s Immunization Record(s) Please make sure that 1) the record also contains your child’s name and birth date.

Related to IMMUNIZATION RECORD

  • Immunization B11.01 The Employer shall provide the employee with immunization against communicable diseases where there is a risk of incurring such diseases in the performance of his duties.

  • Education Record An education record as defined in the Family Educational Rights and Privacy Act and its implementing regulations, 20 U.S.C. 1232g and 34 C.F.R. Part 99, respectively.

  • Education Records Educational Records are official records, files and data directly related to a student and maintained by the school or local education agency, including but not limited to, records encompassing all the material kept in the student’s cumulative folder, such as general identifying data, records of attendance and of academic work completed, records of achievement, and results of evaluative tests, health data, disciplinary status, test protocols and individualized education programs. For purposes of this DPA, Education Records are referred to as Student Data. Personally Identifiable Information (PII): The terms “Personally Identifiable Information” or “PII” has the same meaning as that found in U.C.A § 53E-9-301, and includes both direct identifiers (such as a student’s or other family member’s name, address, student number, or biometric number) and indirect identifiers (such as a student’s date of birth, place of birth, or mother’s maiden name). Indirect identifiers that constitute PII also include metadata or other information that, alone or in combination, is linked or linkable to a specific student that would allow a reasonable person in the school community, who does not have personal knowledge of the relevant circumstances, to identify the student with reasonable certainty. For purposes of this DPA, Personally Identifiable Information shall include the categories of information listed in the definition of Student Data.

  • Immunizations (except for those preventive immunizations for routine use in children, adolescents, and adults that have in effect a recommendation from the Advisory Committee on Immunization Practices of the Centers for Disease Control and Prevention);

  • Medical Records Medical records relating to Trial Subjects that are not submitted to Sponsor may include some of the same information as is included in Trial Data; however, Sponsor makes no claim of ownership to those documents or the information they contain. c.

  • Data Analysis In the meeting, the analysis that has led the College President to conclude that a reduction- in-force in the FSA at that College may be necessary will be shared. The analysis will include but is not limited to the following: ● Relationship of the FSA to the mission, vision, values, and strategic plan of the College and district ● External requirement for the services provided by the FSA such as accreditation or intergovernmental agreements ● Annual instructional load (as applicable) ● Percentage of annual instructional load taught by Residential Faculty (as applicable) ● Fall Full-Time Student Equivalent (FFTE) inclusive of dual enrollment ● Number of Residential Faculty teaching/working in the FSA ● Number of Residential Faculty whose primary FSA is the FSA being analyzed ● Revenue trends over five years for the FSA including but not limited to tuition and fees ● Expenditure trends over five years for the FSA including but not limited to personnel and capital ● Account balances for any fees accounts within the FSA ● Cost/benefit analysis of reducing all non-Residential Faculty plus one Residential Faculty within the FSA ● An explanation of the problem that reducing the number of faculty in the FSA would solve ● The list of potential Residential Faculty that are at risk of layoff as determined by the Vice Chancellor of Human Resources ● Other relevant information, as requested

  • Health Records Provider agrees to cooperate with Subcontractor and/or Health Plan to maintain and share a health record of all services provided to a Covered Person, as appropriate and in accordance with applicable laws, regulations and professional standards.

  • Medical Records Retention Grantee will;

  • Statistical Analysis 31 F-tests and t-tests will be used to analyze OV and Quality Acceptance data. The F-test is a 32 comparison of variances to determine if the OV and Quality Acceptance population variances 33 are equal. The t-test is a comparison of means to determine if the OV and Quality Acceptance 34 population means are equal. In addition to these two types of analyses, independent verification 35 and observation verification will also be used to validate the Quality Acceptance test results.

  • Study Population ‌ Infants who underwent creation of an enterostomy receiving postoperative care and awaiting enterostomy closure: to be assessed for eligibility: n = 201 to be assigned to the study: n = 106 to be analysed: n = 106 Duration of intervention per patient of the intervention group: 6 weeks between enterostomy creation and enterostomy closure Follow-up per patient: 3 months, 6 months and 12 months post enterostomy closure, following enterostomy closure (12-month follow-up only applicable for patients that are recruited early enough to complete this follow-up within the 48 month of overall study duration).

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