NEQAS Enrollment Procedure:
LANDBANK Electronic Payment Portal* steps:
1. Go to http://epaymentportal.landbank.com
2. Under Government Institutions, click National Government Agencies.
3. Select Research Institute for Tropical Medicine (RITM).
4. Select Transaction Type: NEQAS PT-MICRO.
5. Fill-out Transaction Form. Enter code for CAPTCHA.
6. Review Transaction Details. If all information are correct, click “Submit”.
7. Choose Payment Option (e.g. LANDBANK ATM card).
8. Tick box for Terms and Conditions. Click “Submit”.
9. At the end of the Payment Details Page, input the following information:
- 10-digit Account Number
- Joint Account Indicator (JAI), and
- Personal Identification Number (PIN)
10. Click “Submit”, then “Print Debit Confirmation”.
11. Click “Close Window” to begin another transaction.
Eligible Client Accounts:
- LANDBANK ATM Cards
- LANDBANK Visa Debit Cards
- BancNet member banks’ ATM/Debit Cards
A minimum transaction fee of P20.00 will be charged per successful transaction (additional P10.00 will be charged when using other BancNet member banks’ ATM/Debit Cards) and a payment confirmation receipt will be provided for your reference.
*If you choose to pay via LANDBANK Electronic Payment Portal, do not forget to send your filled up enrolment form to NEQAS office for Registration.
Download the NEQAS Enrollment Form here.
The continuing emergence of pathogenic microorganisms that are resistant to first-line antimicrobials is a cause of increasing concern. This emergence is associated with higher levels of mortality and morbidity which not only impacts on patients but also increases the burden on health care services as a result of additional diagnostic testing, prolonged hospital stay and increased intensity and duration of treatment.
There is evidence to suggest that more prudent usage of antimicrobials particularly in the treatment of human disease could make a significant impact on the pace and extent to which resistance emerges in microorganisms pathogenic to man. Minimizing the emergence of antimicrobial resistance to second line broad-spectrum antibiotics (such as the five antibiotics listed in PHILHEALTH circular no. 15, series 2006) could be achieved by restricting their use in favor of first line narrower spectrum but effective antibiotics unless there is evidence to prove (i.e. through surveillance data) that significant antimicrobial resistance to the narrower spectrum antibiotics exist. It is therefore essential that surveillance systems such as an antimicrobial resistance surveillance be in place to provide the information necessary to secure an approach to the management of communicable diseases that minimizes morbidity and mortality whilst also containing the emergence of pathogens resistant to antimicrobials. To be effective, such surveillance systems should 1) be focused on diseases of greatest public health importance (i.e. with high mortality and/or morbidity) and where therapeutic options may be severely limited by antimicrobial resistance; 2) include diseases that are readily transmissible (i.e. may give rise to outbreaks and epidemics); 3) provide information on mortality and morbidity attributable to resistant strains of the organism in the context of that attributable to susceptible strains; and 4) provide information for action at the local, intermediate and national levels. To provide reliable and valid information for action: 1) data on culture identification and antimicrobial resistance should be of a consistently appropriate quality hence the emphasis on adherence to international standards in bacteriology; 2) the capture, collation and analysis of data should be in accordance with protocols of appropriate quality and 3) information outputs should facilitate decision-making by clear presentation and timely distribution and should include a commentary on the limitations of the data presented as well as proposals for interventions.
The RITM Institutional Review Board (IRB) is made up of the Technical and Ethical Review Boards which are composed of individuals with diverse backgrounds, whose responsibility is to ensure that the rights and welfare of the research participants are promoted and their safety protected, while encouraging the conduct of ethically sound research. It is the responsibility of the IRB to review the protocol, participants’ information sheets used to obtain informed consent, investigators’ brochure and other materials required to evaluate compliance with international and national ethical guidelines to conduct research.
To read full Investigator guidelines, click here .
Application for Initial Review
Requirements for Review of Amendments
Application for Continuing Review
Report for of Completion or Termination
Quarter Report of SAEs
Protocol Deviation Report