This
document sets out key work over the next year to progress MHRA’s 2013-18
Corporate Plan and how it will respond to the challenges and opportunities
ahead.
These challenges include:
- Section 4 Safe medicines and devices and secure supply in globalised industries where MHRA objectives are stated as:
- Collaborate with other regulators to achieve a convergence of standards and practice, and make better use of global inspection audit and resources.
- Ensure the quality of medicinal products on the market and act to avoid shortages.
- Tackle the increasing risk of the illegal supply of medicines and devices.
- Develop biological standards to underpin manufacturing consistency and dosing accuracy of biologics.
For
more details, see MHRA
Posted by Tim Sandle
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