Aktualności
EMA: Guideline on the requirements for combined vaccines and associations of immunological veterinary medicinal products (IVMPs)
01.08.2013
This document provides guidance on the data requirements to support authorisation of combined vaccines and a claim for the use of two or more IVMPs, each with its own separate marketing
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GMP: New EMA Inspection Requirements on Good Distribution Practices (GDP)
01.08.2013
On 27 June 2013, the EU Commission updated the so-called \"Compilation of Community Procedures on Inspections and Exchange of Information\". This document serves the exchange of information and
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FDA: Guideline - Evaluation and Recommendation of Pharmacopoeial Texts for Use in the ICH Regions on Bulk Density and Tapped Density of Powders - General Chapter (Q4B Annex 13)
01.08.2013
The FDA finally published the ICH harmonised Guideline entitled \"Evaluation and Recommendation of Pharmacopoeial Texts for Use in the ICH Regions on Bulk Density and Tapped Density of Powders -
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EMA: Draft guideline on the evaluation of medicinal products for the treatment of irritable bowel syndrome
25.07.2013
This guideline intends to address the EU regulatory position in the main topics of clinical development of new medicinal products in the treatment of patients with Irritable Bowel Syndrome (IBS). ...
EMA: Guideline on the clinical investigation of medicinal products for the treatment of urinary incontinence
25.07.2013
This guideline considers pharmacodynamic and clinical data required to support indications, dose regimens and durations of therapy for the treatment of urinary incontinence (UI). It applies to the
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EC: Revision of EU Commission guidelines on Good manufacturing Practice Medicinal Products - annex 16
25.07.2013
This Annex provides guidance on the certification by a Qualified Person (QP) and on batch release within the European Economic Area (EEA) of medicinal products for human or veterinary use holding
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GMP: How do I apply for a CEP? An updated guideline of the EDQM provides information
25.07.2013
The EDQM recently published an updated guidance entitled \"Guidance for electronic and paper submissions for certificates of suitability (CEPs) applications\". This document describes in detail
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FDA: Draft Guidance - Cosmetic Good Manufacturing Practices
18.07.2013
This guidance revises the “Cosmetic Good Manufacturing (GMP) Guidelines/Inspection Checklist” by updating it to set forth current practice, and clarify certain topic areas based on recent
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GMP: Risk-based Approach to APIs Consignments without Written Confirmation
18.07.2013
The provisions of the directive are intended to ensure that API manufacturers in non-EU countries exporting into the EU are registered with their local authorities and subject to adequate
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GMP: FDA Safety Communication: New boxed warning for thrombosis related to human immune globulin products.
18.07.2013
The analysis of recent data by the U.S. Food and Drug Administration (FDA) has strengthened the association between the use of intravenous, subcutaneous and intramuscular human immune globulin
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