Source: https://tendernation.io/opportunities/01a13bf3-2ab2-7315-a38f-bfa405fa74c5/yellow-card-promotion-work

awarded GB open procedure Suitable for SMEs

# Yellow Card Promotion Work

[Medicines and Healthcare Products Regulatory Agency](https://tendernation.io/buyers/medicines-and-healthcare-products-regulatory-agency)

Estimated value

£20,000

Published

18 Nov 2016

Deadline

Closed

28 Feb 2015

## Who can bid

- Buyer says suitable for SMEs

    The buyer ticked “suitable for SMEs” on the notice. Anyone can still bid.
- Small contract value

    Valued under £135,018 including VAT, the lowest Procurement Act threshold for goods and services.
- Open procedure

    Anyone can submit a full tender; there is no shortlisting stage.

[More contracts for small businesses and VCSEs](https://tendernation.io/opportunities/for-small-businesses)

## About this tender

This contract is a National Health Service (NHS) contract pursuant to section 9 of the NHS Act 2006 and sets out what Yellow Card promotion work the Provider will undertake each year, through a Yellow Card Centre, in return for payment from the Commissioner.

The aim of the Yellow Card scheme is to monitor the safety of the medicines and vaccines that are on the market.

The Yellow Card Scheme is vital in helping the MHRA monitor the safety of all healthcare products in the UK to ensure they are acceptably safe for patients and those that use them. Reports can be made for all medicines including vaccines, blood factors and immunoglobulins, herbal medicines and homeopathic remedies, and all medical devices available on the UK market.

The Scheme collects information on suspected problems or incidents involving

1.side effects (also known as adverse drug reactions or ADRs)

2.medical device adverse incidents

3.defective medicines (those that are not of an acceptable quality)

4.counterfeit or fake medicines or medical devices

It is important for people to report problems experienced with medicine or medical devices as these are used to identify issues which might not have been previously known about. The MHRA will review the product if necessary, and take action to minimise risk and maximise benefit to the patients. The MHRA is also able to investigate counterfeit or fake medicines or devices and if necessary take action to protect public health.

Read full description

## CPV classification

Medical information systems

Source

Contracts Finder (UK)

[View official notice](https://www.contractsfinder.service.gov.uk/notice/43f1b494-adc9-11e6-9901-0019b9f3037b)

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