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A Message from MIAS Pharma (COVID – 19)

2020-04-07T14:15:30+01:00

I wish to update you on MIAS Pharma ltd position regarding COVID-19. The World Health Organisation formally declared COVID-19 a pandemic, and the European Centre for Disease Prevention and Control (ECDC) updated its guidelines around the importance of early intervention. While continuing to conduct business in these challenging times it is our priority to reduce [...]

A Message from MIAS Pharma (COVID – 19)2020-04-07T14:15:30+01:00

EU: First steps taken to diminish drug shortages

2019-09-10T09:55:50+01:00

Regulators in the European Union (EU) have began taking the first steps reduce shortages of medicinal products. The European Medicines Agency (EMA) and the Heads of Medicines Agencies (HMA) recently published two guidance documents. The two guidance documents are said to be used as a foundation. The first guidance document that has [...]

EU: First steps taken to diminish drug shortages2019-09-10T09:55:50+01:00

Brexit: Industry should keep Timelines for Batch Testing Facilities

2019-08-01T16:13:35+01:00

A reminder was sent out to stakeholders of the European Medicines Agency (EMA) which pointed out that, independent from the extension of the date for the UK’s withdrawal from the EU (Brexit) to the 31st of October 2019, Marketing Authorisation Holders (MAH’s) should use the remaining time to complete all necessary preparations. [...]

Brexit: Industry should keep Timelines for Batch Testing Facilities2019-08-01T16:13:35+01:00

The meaning of Market Access

2019-07-31T09:59:19+01:00

Market Access is the process to ensure that all appropriate patients who would benefit, get rapid and maintained access to the brand at the right price. Understanding the process: It is important to understand all the processes that impact market access, both internal and external: Payers have processes – at national level [...]

The meaning of Market Access2019-07-31T09:59:19+01:00

A milestone has been reached by the EU and US (MRA)

2019-07-17T11:28:47+01:00

With the recognition by the US Food and Drug Administration (FDA) of Slovakia, the European Union and the United States have now fully implemented the mutual recognition agreement (MRA) for inspections of manufacturing sites for certain human medicines in their respective territories. Each year, EU national authorities and the FDA inspect many [...]

A milestone has been reached by the EU and US (MRA)2019-07-17T11:28:47+01:00

Construction begins on €325m WuXi Biologics plant in Dundalk

2019-06-04T14:57:57+01:00

Construction has begun on the €325m WuXi Biologics plant in Dundalk which aims to be the world’s largest single-use biologics manufacturing facility. WuXi Biologics is Chinas leading end-to-end biologics solutions provider with the Dundalk campus and is set to be its first manufacturing facility outside China. The build is on schedule for [...]

Construction begins on €325m WuXi Biologics plant in Dundalk2019-06-04T14:57:57+01:00

Brexit: Will UK Inspection Reports and GMP Certificates still be valid?

2019-03-01T10:42:34+00:00

The European Medicines Agency (EMA) has updated the agency’s Brexit-related guidance documents. The updated documents support pharmaceutical companies in preparing for the United Kingdom’s (UK) withdrawal from the European Union (EU). All medicinal products that are manufactured or imported into the European Economic Area (EEA) must be follow EU Good Manufacturing Practices [...]

Brexit: Will UK Inspection Reports and GMP Certificates still be valid?2019-03-01T10:42:34+00:00

UK amends GMP and GDP Regulations

2019-02-01T14:10:03+00:00

There is still a very strong possibility that there will be a “Hard Brexit”. The term “Hard Brexit” refers to the United Kingdom leaving the European Union without a deal. The UK Government is now preparing legislation to allow the continued sale of and access to medicines manufactured in the remaining EU. [...]

UK amends GMP and GDP Regulations2019-02-01T14:10:03+00:00
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