13 February 1996
ADMINISTRATIVE ORDER
No. 4 series 1996
STANDARDS
FOR BLOOD BANKS AND BLOOD CENTERS IN THE PHILIPPINES
Pursuant to Section 9 of
R.A. 7719, otherwise known as the “National Blood Services Act of 1994,”
and Section 26 and 38 of its Implementing Rules and Regulations (DOH A.O.
No. 9 series of 1995) the attached First Edition 1996 of the “Standards
for Blood Banks and Blood Centers in the Philippines” is hereby
incorporated as an integral part of the Implementing Rules and Regulations of
R.A. 7719.
Section 1
This shall be known as the
“Standards for Blood Banks and Blood Centers in the Philippines.”
Section 2
Purpose
These standards are issued
to define the level of desirable services in Blood Banks and Blood Centers in
the country. It is envisioned that adherence to these will lead to quality
service and the safety of blood and blood products for all patients.
These standards describe
the mandatory and recommended practices for blood banks and blood centers.
Specific Licensing
Requirements and Procedures shall be issued as subsequent Bureau Orders or
Memorandum Circulars from the Bureau of Research and Laboratories, Department
of Health.
Section 3
Scope
These Standards shall
apply to all Blood Banks and Blood Centers whether hospital or non–hospital
based, within the geographical boundaries of the Philippines
Section 4
Dissemination
To ensure that relevant key
persons are informed of these Standards and subsequent revisions, all Regional
Health Directors, Chiefs of Hospitals and all heads of licensed blood
banks/blood centers shall signify knowledge of these Standards through
appropriate acknowledgement receipts and memos. The heads of the blood banks/centers
are responsible for making sure that these Standards are read and understood by
all concerned blood bank/blood center staff.
Section 5
Violations
Non–compliance of these
Standards shall be regarded as a violation under R.A. 7719 and thus is subject
to the penalties defined by R.A. 7719 and Department of Health A.O. No. 9 s.
1995.
Section 6
Repealing Clause
These Standards supersede all
previous Department and Bureau Orders, Circulars and Memoranda (A.O. No. 57, s.
1989; B.O. No. 5, s. 1990, A.O. No. 122, s. 1992; Bureau Circular No. 2, s.
1990, No. 2, s. 1991 and No. 4, s. 1994 of the BRL). The provisions of any
Department or Bureau issuances inconsistent with these Standards are hereby
nullified.
Section 7
Effectivity Clause
These standards shall take
effect immediately.
Full enforcement shall
commence on January 1, 1997. Year 1996 will considered a transition period for
all concerned to upgrade their capabilities for meeting the Standards.
There shall be reviewed
and if necessary, revised, by the Bureau of Research and Laboratories (BRL),
every two (2) years. Revised editions shall have clearly stated effectivity
dates and shall be signed by the BRL Director. All previous editions shall be
recalled by the BRL.
HILARION J. RAMIRO,
JR., M.D., MHA
Secretary of Health
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