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New FDA Regulation gives the Agency more Power during an Inspection

12.09.2013
The U.S. Food and Drug Administration (FDA) is proposing a regulation to implement administrative detention authority during inspections. ...

Specification of the Unique Facility Identifier (UFI) System for Drug Establishment Registration

12.09.2013
This guidance specifies the unique facility identifier (UFI) system for registration of domestic 20 and foreign drug establishments. ...

EXCiPACT - Pilot Phase Successfully Completed!

12.09.2013
EXCiPACTTM is a quality standard for the manufacture, storage and transport of excipients which is now recognised by authorities and the industry worldwide. It has been made available to the ...

New FDA Fees for Drug Master Files published

12.09.2013
The US FDA has published the new fees for 2014. In a Federal Register Statement dated August 2, 2013 the following information has been published: Under the Generic Drug User Fee Act (GDUFA), the ...

GMP: EMA publishes Guideline on Pharmaceutical Development of Medicines for Paediatric Use

05.09.2013
The European Medicines Agency has published the final Guideline on pharmaceutical development of medicines for paediatric use. The date for coming into effect is 15 February 2014. ...

FDA: Draft Guidance for Industry and Food and Drug Administration Staff - Medical Device Reporting for Manufacturers

05.09.2013
Because of the number and complexity of medical devices, FDA\'s Center for Devices and Radiological Health (CDRH) has published many new guidelines. The \"Draft Guidance for Industry and Food and ...

FDA: Guidance for Industry and FDA Staff: - Technical Considerations for Pen, Jet, and Related Injectors Intended for Use with Drugs and Biological Products

05.09.2013
This guideline addresses specific application systems with regard to combination products. The guideline deals with aspects relevant for a marketing authorisation and expected by the FDA in a ...

GMP: ASEAN Countries publish Draft of a Guideline on Process Validation

05.09.2013
The member states of the Southeast Asian association (ASEAN) have released the draft of a process validation guideline under the management of Singapore. Members of the ASEAN countries are: ...

EMA: Draft policy 70: Publication and access to clinical-trial data

05.09.2013
There is growing demand from external stakeholders for full transparency, not only about the European Medicines Agency\'s deliberations and actions, but also about the data and results from ...

EMA: Guidance on format of the risk-management plan in the European Union – in integrated format

29.08.2013
This guidance covers the Parts and modules of the RMP which may be required for applications in the EU. ...