Aktualności
GMP: Current FDA Publications for Medical Device Manufacturers
04.09.2015
In irregular intervals, the ECA publishes overviews of the FDA\'s new guidances or draft guidances, webinars, general strategy papers and inspection results concerning medical devices. The
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URPL: Information of President of The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products of August 20, 2015 concerning the interpretation of the term specified in the Ordinance of the Minister of Health of 5 November 2013
04.09.2015
This document is announcement of President of The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products of August 20, 2015 concerning the interpretation of the term
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FDA: Brief Summary and Adequate Directions for Use: Disclosing Risk Information in Consumer-Directed Print Advertisements and Promotional Labeling for Prescription Drugs
20.08.2015
This revised draft guidance provides recommendations on the disclosure of risk information in prescription drug product advertisements and promotional labeling in print media directed toward
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FDA: Rare Diseases: Common Issues in Drug Development
20.08.2015
This guidance assists sponsors of drug and biological products intended to treat or prevent rare diseases in conducting more efficient and successful development programs through a discussion of
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RAPS: Pakistani Manufacturers Shut Down in Protest Against Regulatory Amendment
20.08.2015
Members of the Pakistan Pharmaceutical Manufacturers Association (PPMA) have shut down their units in protest against regulatory changes. The actions were later postponed following the death of a
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EMA: Guideline on good pharmacovigilance practices (GVP) - Module VIII – Post-authorisation safety studies (Rev. 2)
20.08.2015
A post-authorisation safety study (PASS) is defined in Directive 2001/83/EC (DIR) Art 1(15) as any study relating to an authorised medicinal product conducted with the aim of identifying,
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EMA: Guideline on good pharmacovigilance practices (GVP) - Module VIII Addendum I – Requirements for transmission of information on non-interventional post-authorisation safety studies (Rev. 2)
20.08.2015
This addendum specifies requirements for the transmission of study protocols, updated protocols following substantial amendments, final study reports and progress reports if requested on
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EMA: Guideline for good clinical practice E6(R2) 4 - Step 2b
13.08.2015
Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects.
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EMA: Draft guideline on the processing of renewals in the centralised procedure
13.08.2015
This guideline considers issues associated with the processing of renewals in the centralised procedure, with an aim of giving procedural guidance to marketing authorisation holders (MAHs). It has
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FDA: Dissolution Testing and Specification Criteria for Immediate-Release Solid Oral Dosage Forms Containing Biopharmaceutics Classification System Class 1 and 3 Drugs
13.08.2015
This guidance is developed to provide manufacturers with recommendations for submission of new drug applications (NDAs), investigational new drug applications (INDs), and/or abbreviated new drug
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