Good Manufacturing Practice Analysis and Testing Training
key details
| Value | £27,200 |
|---|---|
| Status | complete |
| Category (CPV) | 80000000 |
| Region | London |
| Deadline | 20 Jan 2023 |
| Contract start | 13 Feb 2023 |
| Contract end | 31 Mar 2023 |
| Procedure | direct |
| SME suitable | Yes |
| OCID | ocds-b5fd17-61ca0794-5969-44c8-9bae-b1c0f335cfde |
Award
| Supplier | Value | Date | Status |
|---|---|---|---|
| NSF Health Sciences Ltd | £27,200 | 27 Feb 2023 | active |
description
The MHRA require classroom training on the subject of Good Manufacturing Practice of Pharmaceuticals and the analysis and testing of these products. This course will provide technical knowledge around the analytical chemistry techniques for up to 20 inspectors who require this training to fulfil the role of regulatory inspections of laboratories performing batch release testing of pharmaceuticals.
Training of this type forms part of the training for a Qualified Person (QP) as described by HMR 2012 which is a key role named on MHRA issued authorisations fundamental to ensuring the safety of medicines.
notice history
1 notice published against this procurement.
| Published | Type | Regime | Notice |
|---|---|---|---|
| 28 Feb 2023 | Award (award) | · | 3d5d8ee3-fefe-4c61-a02c-d088c27293de-619453 |
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source
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