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| Original News Release |
The Pharmaceutical Task
Force’s report made 12 recommendations to government regarding PharmaCare’s
policy, programs, services and drug approval process.
Recommendation 1 – Priority attention should be focused on development of an enhanced
Formulary Management System together with improved stakeholder engagement and
appeal mechanisms. This work should be led by the Pharmaceutical Services
Division and include meaningful engagement with stakeholders, including
patients, healthcare professionals, disease specialists, research leaders and
industry.
Recommendation 2 – The Ministry of Health should act to establish new target
review/listing decision guidelines with the goal of substantially improving
B.C.’s performance on time-to-listing decisions. Progress on this front must be
publicly reported and consistently benchmarked against the performance of other
jurisdictions.
Recommendation 3 – The Drug Benefit Committee should be reconstituted as the Drug
Benefit Council to more appropriately reflect the arm’s-length role it is
expected to carry out in the review processes applicable to consideration of
new therapies.
Recommendation 4 – The Ministry of Health should establish a new Drug Review Resource
Committee (DRRC) to carry out the drug submission review role currently
performed by the Therapeutics Initiative. This new DRRC should also provide for
a registry of experts that will substantially widen the array of expertise
available to offer advice and recommendations on the therapeutic value and
cost-effectiveness of new drug therapies.
Recommendation 5 – The membership of the Drug Benefit Committee should be modified to
include the participation of at least three public members selected through a
process external to the Pharmaceutical Services Division. Government may also wish to consider
ensuring that at least one member of the Drug Benefit Committee has broad
economic expertise to supplement the existing expertise that is focused more
narrowly on health economics.
Recommendation 6 – No members of the Therapeutics Initiative or, in the alternative, no
participant in a Drug Coverage Review Team should participate as members in the
work of the Drug Benefit Council.
Recommendation 7 - The Pharmaceutical Services Division should initiate a negotiation
process with drug manufacturers and with representatives of community pharmacy
and pharmacists to establish new price and reimbursement arrangements and
increased competition in respect of generic pharmaceutical products. If the parties
are unable to conclude an acceptable agreement within six months, the
government should move unilaterally to address the needs of the Province
through legislation or through other means.
Recommendation 8 – To increase the level of overall funding transparency, negotiations
with pharmacists and community pharmacy should provide for a new framework for
compensation in respect of dispensing and other professional services provided
by pharmacists. The framework should address those professional services that
can be effectively and efficiently provided by pharmacists and should be linked
to transparent accountability agreements to maintain and, ideally, improve
point-of-care services to patients.
Recommendation 9 – The Pharmaceutical Services Division should adopt a cautious
approach to broadened utilization of tendering processes. The process adopted
should mirror tendering processes used in other areas of government
characterized by a process that is transparent, fair, open and includes
understandable evaluation criteria. Increased tendering should provide for
reasonable levels of patient choice, avoid the deployment of older inferior
products and, where possible, arrangements that provide for participation of
multiple suppliers.
Recommendation 10 – The deputy minister of the Ministry of Health should commit to
participate in an annual accountability session to hear from patient groups,
from industry and from other key stakeholders regarding improved relations and
the strengthening of the common objectives of patient care and choice.
Recommendation 11 – Given that B.C. was a lead jurisdiction in calling for the
implementation of the Common Drug Review, action should be taken to:
·
Ensure B.C.’s
decision-making processes include similar timelines to those used by the Common
Drug Review and a greater level of
commitment to openness and transparency; and
·
That any unnecessary
overlap between the Common Drug Review and B.C. formulary management system are
reduced to the fullest extent possible.
Recommendation 12 – Subject to Recommendation 4, if the Therapeutics Initiative (TI) is
maintained, action must be taken in the following areas:
·
The governance,
membership and accountability standards associated with the operation of the TI
will require substantial improvement;
·
Steps must also be taken
to renew and revitalize the panel of experts the TI relies upon to discharge
its obligations;
·
The function of the TI
should be focused on therapeutic evaluation. Activities beyond that core
mandate, such as public education, should be reassigned to the ministry’s Drug
Utilization Branch where an accountable process can be implemented to assure
unbiased and evidence-based practices;
·
The practice of having
members of the Therapeutics Initiative also participating in the work of the
Drug Benefit Committee should be terminated.
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contact: |
Manager, Media Relations Ministry of Health 250 952-1887 (media line) |
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