Good Manufacturing Practice Analysis and Testing Training
A Contract Award Notice
by MEDICINES AND HEALTHCARE PRODUCTS REGULATORY AGENCY
- Source
- Contracts Finder
- Type
- Contract (Services)
- Duration
- 1.5 month
- Value
- £27K
- Sector
- PROFESSIONAL
- Published
- 28 Feb 2023
- Delivery
- 13 Feb 2023 to 31 Mar 2023
- Deadline
- 20 Jan 2023 12:00
Concepts
Location
1 buyer
1 supplier
- NSF Health Sciences York
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.
Award Detail
1 | NSF Health Sciences (York)
|
CPV Codes
- 80000000 - Education and training services
Indicators
- Contract is suitable for SMEs.
Other Information
C126738 Good Manufacturing Practice of Pharmaceuticals Training - PO REDACTED C126738 Good Manufacturing Practice of Pharmaceuticals Training - PO REDACTED.pdf
Reference
- CF-1369700D0O000000rwimUAA
- CF 3d5d8ee3-fefe-4c61-a02c-d088c27293de