Procurement and Distribution Interest Group
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Recent changes to quality assurance assessment of
licensed medicines were among the topics discussed at the Procurement
and Distribution Interest Group of the Guild of Healthcare Pharmacists’ autumn
symposium. Matthew Wright reports |
This article as a PDF (70K) |
The autumn symposium
of the Procurement and Distribution
Interest Group of the Guild
of Healthcare Pharmacists was held in Coventry on
2 November 2006.
Matthew Wright is news and feature writer for The
Pharmaceutical Journal. Procurement of pharmaceuticals was the
subject of last month’s Hospital Pharmacist Special Feature (2006;13:391–403). |
Procuring quality medicines
Quality assurance (QA) assessment of licensed medicines is currently moving
away from a focus on laboratory analysis, towards more of a risk assessment
approach, Richard
Bateman, quality assurance specialist pharmacist, London region, told attendees.
“Over the past few years we have really developed and formalised the
way we get QA input into the procurement process,” he said. There is
now more of a focus on identifying the potential for medication errors and
ensuring
that products are safe in use.
Mr Bateman explained that this new focus was linked to the introduction of
the Supply Chain Excellence Programme, which led to the development of a nationally
co-ordinated approach and the concept of “purchasing for safety”.
A contract award criteria has been established which links
in with QA assessment processes, he explained.
Mr Bateman said that a better relationship has now developed between QA and
procurement pharmacists, the NHS Procurement and Supply Agency (NHS PASA),
and the National Patient Safety Agency. The NHS Pharmaceutical Quality Assurance
Committee produces guidance documents for the NHS, including “Quality
assurance and risk assessment of licensed medicines for the NHS”, published
in 2004. Mr Bateman added that a procurement subcommittee was formed to manage
the QA assessment process.
The assessment process largely considers safety of medicines in use, he said.
Product samples (or an accurate mock-up) are allocated to QA pharmacists across
the UK for assessment. An overall assessment, comments and images are collated
and presented for adjudication. Risk assessment
of pharmaceuticals being evaluated for NHS contracts includes consideration
of issues such as medication error potential (eg, products with similar appearance
or names), product quality and fitness for purpose (eg, ease of opening) and
manufacturer performance assessment (eg, reliability, number of recalls).
Collaborative hubs
Chris Theaker, newly appointed director of procurement, pharmaceuticals, at
NHS PASA, described how the Collaborative Procurement Hubs (CPH) project is
working with trusts and confederations in a phased approach to develop CPHs
across the NHS that provide a regional procurement focus. He said that procurement
hubs would be become more formal in structure. “By 2008 we anticipate
there being national coverage in terms of procurement groups … to coincide
more with the 10 strategic health authority boundaries,” he added.
He said that CPHs are designed to provide a consistent approach to purchasing,
provide a resource for sourcing and supply chain development, drive value and
engage with stakeholders throughout the whole commercial process.“I hope
that those of you who are working in the NHS would be aware of … where
the hubs are evolving, who the contact points are and how your local procurement
organisation would fit into the hub structure,” he added.
New NHS specials database
A decision support tool to help NHS pharmacy staff identify and source unlicensed
products made by NHS manufacturing units was previewed by Tim Root, specialist
pharmacist, clinical governance and technical services for London, East and
South East specialist pharmacy services.
The web-based Pro-File database contains a product list, which currently stands
at about 2,500 lines, and includes core data for all products that are being
manufactured and used by the NHS. Mr Root said that Pro-File will offer would-be
purchasers a list of contact details of all manufacturers on the Medicines
and Healthcare products Regulatory Agency’s register of manufacturers
holding a specials licence.
Mr Root said: “Access to Pro-File is by registration and only bona
fide NHS pharmacy staff with an NHS e-mail address are eligible to register. The
site will only include product data from NHS manufacturing units and will not
be accessible
outside the NHS.”
He also made it clear that Pro-File is not an ordering system and that the
final decision about what to buy and from where is entirely the purchaser’s.
NHS manufacturing units currently have access to the database and are in
the process of adding their inventories.
“The quality and scope of the product-specific information, such as pack
size, label details, excipient details and formulation information, is entirely
down
to the manufacturer; there is an expectation that all licensed NHS manufacturers
will contribute their data,” Mr Root said.
Innovation in pharmacologistics award

Kirsty Docherty |
During the symposium, the 2006 Guild of Healthcare Pharmacists’ “Innovation
in pharmacologistics” award, sponsored by Pfizer, was presented to Kirsty
Docherty (pictured).
Ms Docherty, procurement services manager at University College London Hospitals
NHS Foundation Trust, is to use the £1,500 prize money to undertake a
review into the purchasing and contracting practices of medicines consortia
when dealing with branded medicines.
She aims to develop a range of key
performance indicators that can be used throughout the UK. |