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NSF’s pharmaceutical industry update looks at changes in guidelines and legislation that will impact the pharmaceutical sector.
This edition looks at:
Detailed legislation updates are also available on the NSF Pharma App.
The European Medicines Agency (EMA) published a draft reflection paper on January 14, 2020, on the GMP-related responsibilities that apply to marketing-authorization holders (MAHs), with a deadline for comments on April 14, 2020. The final version was published as part of Part III of the EU GMP Guide on July 23, 2021.
The reflection paper makes it clear that even if the MAH is not directly engaged in the manufacture of products under EU law and the GMP guide, they do still have GMP responsibilities. The EMA seeks to clarify the various responsibilities and what they mean for MAHs at a practical level. As outlined in this paper, while certain activities of an MAH may be delegated to a manufacturer or other party, the MAH retains the ultimate responsibility for the performance of a medicinal product over its lifetime, including its safety, quality and efficacy.
The paper points out that Article 111 of Directive 2001/83/EC and Article 80 Directive 2001/82/EC give powers to Member State authorities to inspect the premises of MAH companies. This reflection paper may serve as useful guidance for the competent authorities performing the inspections.
Section 4 of the paper outlines the MAH’s role in facilitating compliance with GMP and the marketing authorisation (MA). These responsibilities generally relate to:
Section 5 of the paper, which forms the bulk of the 29-page document, outlines each GMP requirement that applies to the MAH. The requirements are grouped together under a number of different themes:
Section 6 outlines the directive on falsified medicines and MAH responsibilities relating to safety features.
The ICH Assembly endorsed the topic of continuous manufacturing (CM) in June 2018 and an expert working group was formed. The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) brings together regulatory bodies and the pharmaceutical industry to develop ICH Guidelines.
The draft of Q13 gained step 2b approval and was issued for public comment. Step 3 of the ICH process began on July 27, 2021. In Europe, the deadline for comments is December 20, 2021. Q13 is intended to apply to drug/medicinal products and drug substances/APIs for chemical entities and therapeutic proteins. The principles may also apply to other biological and biotechnological entities. CM applies to new products and the conversion of batch manufacturing to CM for existing products.
Section 2 of the draft guideline describes three different models of CM:
The draft uses the ICH Q7 definition of a batch for both drug substance and drug product. Based on this definition, the size of a batch produced by CM can be defined in terms of one of the following:
Batch size can also be defined as a range. Other approaches to defining batch size can be considered if scientifically justified.
Section 3 of the draft guidelines covers scientific approaches, outlining control strategy development, production output changes and continuous process verification.
Section 4 itemizes regulatory considerations, and section 5 is a glossary of key terms.
Part 2 of the draft is a series of five annexes comprising more than half of the document. The annexes cover:
The Pharmaceutical Inspection Co-operative Scheme (PIC/S) published the “COVID-19 Risk Assessment for National Routine On-Site Inspections” on July 15, 2021.
The 12-page guidance document is to be completed by inspectors during the planning phase of inspections. The site to be inspected must then confirm that all necessary measures identified in the risk assessment will be implemented.
NSF’s expert team works with companies around the world to ensure their manufacturing processes are compliant with necessary legislation and regulations. We can:
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