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Question of the Week

Question of the Week | GMP-Verlag

What are the individual steps of an efficient QRM process?

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How is a QRM process initiated?

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What should be considered in risk assessment?

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What are the quality requirements for pharmaceutical gases?

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What are the requirements for gas distribution systems?

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What is a gas?

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What is a Certificate of Analysis (COA)?

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What is essential for the structure of container closure systems used for product packaging?

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What are the elements of a computerised system?

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Which materials can be used for furniture and furnishings in cleanliness Grade C?

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What is the purpose of line clearance?

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What is a training profile?

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What is the purpose of a measurement point risk analysis?

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What does the catchphrase "Supply Chain Integrity" mean?

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What are the main tasks of the Head of Quality Control?

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What are the advantages and benefits of quality risk management (QRM)?

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Who is responsible for qualification?

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What is monitoring?

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How can conformance with GMP requirements for active substances be proven?

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What is the dual function of protective clothing in pharmaceutical manufacturing?

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Why is a system suitability test (SST) performed in addition to equipment qualification?

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Which test is used to determine the conductivity of pharmaceutical water qualities?

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What is a validation test?

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How do files and dossiers differ from each other?

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Where can I find specific information on the subject of "transport and temperature"?

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Why does the performance qualification of a water supply system take one year?

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How do APR and PQR differ in terms of the number of batches to be assessed in the review period?

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What does Annual (Product) Review mean?

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What are the 3 main types of safety features against drug counterfeiting?

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What role does quality risk management play in the quality management system?

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How do you ensure the traceability of the batch documentation?

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Which filters are used in safety cabinets, and which filter tests are to be carried out?

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Who is responsible for establishing the Pharmaceutical Quality System and making it work?

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For what purposes are insulators used?

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What is adjustment?

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Why does it take a year to qualify the performance of a water supply system?

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What is rouging and how do you deal with the problem?

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What are endotoxins?

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What should be considered when installing automatic sliding doors in cleanrooms?

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To which areas does the self-inspection refer?

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What information should be covered by the validation report?

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What are the disadvantages of using activated charcoal filters in water treatment?

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What general hygiene measures need to be observed?

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What is an action limit, and what happens when it is exceeded?

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What are the concepts for protecting clean work areas?

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How should change management be documented?

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Why is batch-specific identification necessary and how is it done?

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What is the difference between a bubble type and a sink type pressure cascade?

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What should you bear in mind when maintaining rooms?

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What is meant by adjustment?

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How does a risk assessment work?

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What has to be considered when releasing batches with deviations?

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What are the powers of the GMP inspectors in inspections?

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What are the most important QMS areas of a GMP inspection?

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What is the difference between a correction and a corrective action?

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What is the difference between an EU regulation and an EU directive?

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What are the risks associated with microbiological monitoring?

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What is the goal of supplier qualification?

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What formal aspects help to improve the readability of SOPs?

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What is the purpose of a qualification audit?

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What is the purpose of stability testing?

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How do you develop a process management and control strategy?

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What is the objective of laboratory equipment qualification?

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What is a Contamination Control Strategy (CCS) and what does it include?

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Why is the use of activated carbon filters critical as a pre-treatment process?

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What are the objectives of personnel medical examinations?

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What is the purpose of self-inspections?

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What are the pros and cons when using UV irradiation in water pre-treatment systems?

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Question of the Week | GMP-Verlag

Can operators of existing systems for the production of highly purified water (HPW) still refer to the Ph. Eur. now that HPW is no longer listed there?

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What is a static form?

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Question of the Week | GMP-Verlag

Which quality and process parameters must typically be taken into account during process validation for terminally sterilized products?

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What does reworking mean in the production of APIs?

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What types of cabinets are available?

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What requirements for "Good Distribution Practice" can be found in national and international regulations?

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What general hygiene measures need to be observed in storage areas?

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Question of the Week | GMP-Verlag

Why is temperature a critical aspect in transportation?

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When is qualification required for rooms and air handling units and when is technical acceptance testing sufficient?

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What are the phases that characterise the life cycle of a computerised system?

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What is the function of metadata for document management?

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Which GMP inspection types can be distinguished?

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What requirements must cleaning processes meet in terms of cleaning validation?

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Which phases characterise the life cycle of a computerised system?

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What types of requalification are distinguished?

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What is the difference between the clean up period according to Annex 1 and the recovery time according to ISO 14644-3?

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What types of CIP systems are used in practice?

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What are the possible benefits of risk management in transportation?

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What does a company that has incorporated a proactive compliance program look like?

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What means Limit of Quantitation (LOQ)?

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What contracts are usually concluded in outsourcing?

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What does calibration mean?

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Question of the Week | GMP-Verlag

What activities does the distribution of active ingredients involve?

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What information should be included in the validation plan?

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What is the difference between a direct cause and a contributing cause of failure?

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What is an ASMF?

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What are the 6 different types of Excel applications?

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What is meant by import?

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What is the significance of an alert level?

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What is the purpose of process visualisation?

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What does reprocessing mean in the production of APIs?

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What are isolators and what are they used for in the pharmaceutical industry?

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At what point may water be used during the performance qualification of a water supply system?

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What is calibration?

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How should one handle qualification data?

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Who is responsible for the implementation of a Batch Record Review?

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Question of the Week | GMP-Verlag

In outsourcing, who is responsible for the quality of the medicinal products produced?

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Question of the Week | GMP-Verlag

What are the 3 designs for counterfeit-proof features?

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How are medicinal products requiring cool transport conditions labeled for air freight?

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What factors influence cleaning?

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Question of the Week | GMP-Verlag

What is a computerised system?

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What is an alert limit, and what happens when it is exceeded?

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What is hygienic design?

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Should calibration be done during IQ or as part of OQ?

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Question of the Week | GMP-Verlag

How can the specific requirements for sterile products be taken into account in the quality management system?

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What must be observed when planning and designing distribution systems for pure steam?

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Question of the Week | GMP-Verlag

What four phases should the development of a cleaning process ideally go through?

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What is an end-to-end verification system?

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What information must be included in the microbiological monitoring plan?

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What special features need to be considered when determining the total microbial count in pharmaceutical water?

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From what stage in the chemical manufacturing process do GMP regulations apply?

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What are complexing agents and how do they work?

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In which countries do the GMP rules for active ingredients according to ICH Q7 apply?

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What are the spatial requirements for the incoming goods and dispatch areas?

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Is there a difference between pharma monitoring and I&C system?

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Why do analytical test methods need to be validated?

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What is the significance of an action level?

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Do USP methods need to be validated by the user?

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What is commissioning?

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What is DIN Spec 91323?

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What are the central tasks of logistics?

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Who is responsible for planning and implementing cleaning validation?

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Which categories of documents do the EU GMP Guidelines identify?

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What is the validation of a computerised system?

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Who developed the fishbone diagram?

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What is the importance of plant design for qualification?

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What does line clearance mean?

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Which aspects are decisive for the performance of passive shipping containers?

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What are the advantages and disadvantages of in-line measurement of the conductivity of water for injection (WFI)?

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What is gauging?

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What is the difference between a corrective action and a preventive action?

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What data is monitored when monitoring a HVAC system?

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What are the responsibilities of the Qualified Person according to EU Annex 16?

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What determines the level of effort, rigour and formality with which QRM is applied?

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Is it acceptable to use a transport trolley for material transfer from one cleanliness class to another?

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Which spray heads can be used in CIP systems?

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What needs to be taken into account when using and maintaining safety cabinets?

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How does ultrafiltration work?

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Do European Pharmacopoeia methods need to be validated by the user?

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What are print data for secondary packaging materials?

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Which product groups are included under the term immunological medicinal products?

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How can a sterilisation process be checked?

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What is a deviation?

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How should the qualification be documented?

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How is a physicochemical monitoring program structured?

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What is an active pharmaceutical ingredient (API)?

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What do the authorities expect during the first inspections after the revised Annex 1 came into force?

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What is the disadvantage of a sit-over bench?

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Who is responsible for the existence and effectiveness of deviation management?

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What is a training profile? (2018)

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Which two factors are particularly important for a GMP-compliant process validation?

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How are deviations defined?

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What is meant by archiving?

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What is the difference between the point of occurrence and the point of recognition of a failure?

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For what purposes can drinking water be used in the pharmaceutical industry?

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Who is responsible for generating the PQ protocols?

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What are immunological medicinal products?

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How does electro-deionisation work?

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What is meant by serialisation?

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What is the link between the European and the British Pharmacopoeia?

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What are the steps of an inspection procedure?

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What is an OEL value?

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What is the official document containing official actions sent by the FDA after a GMP inspection called?

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What options are there for evaluating the Quality System?

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What is the EMA and what tasks does it fulfil?

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Which key aspects should be addressed when defining the requirements profile of a logistics service provider?

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What is RAN and what is its purpose?

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What does official calibration mean?

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What are the advantages of a dynamic e-form?

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Why should inactivating agents be added to the culture media when performing tests for microbiological monitoring?

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When is a determination of the conductivity useful in cleaning validation?

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What must the data owner ensure regarding data archiving?

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Which metrics are subject to monitoring?

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Which GxP critical aspects are affected when storing data in the cloud?

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What is an alert limit?

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What is a verified copy?

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What is a Biosafety Level (BSL)?

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What are the main tasks of the Head of Production?

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What is a true copy?

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What quality requirements must pure steam meet?

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Which persons are responsible for storage in the GMP or GDP area?

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Where can you find concrete information regarding "transport and temperature?"

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How can the suitability of premises be verified?

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What does commissioning mean?

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What is metrology?

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What is the EDQM and what are its tasks?

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For what purposes are isolators used?

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Under what conditions may a contract acceptor subcontract activities to third parties?

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What are the advantages of using Ultrafiltration?

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What is a shared audit?

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What must be observed when working with gloves in isolators?

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To which products does the new Annex 21 to the EU GMP Guide apply?

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Why should OQ tests cover the entire working range of the equipment?

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Which processes are available for reduction of microbial counts in water systems?

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What are the major trends that have recently changed the concept of validation?

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What requirements are placed on cleanroom personnel?

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Where do SOPs need to be available?

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Is it reasonable to test purified water for the presence of E. coli?

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What is an excipient?

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What has to be considered for risk management?

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What is pharmacovigilance?

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What is the purpose of a general GMP inspection?

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What is meant by registration or authorisation batches?

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What are the advantages and disadvantages of the rinse test for cleaning validation?

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What are the requirements for successful quality risk management (QRM)?

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Which countries are covered by the British Pharmacopoeia?

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What is the official document containing official actions sent by the FDA after a GMP inspection called? | 2022

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How can a uniform colouring of secondary packaging materials be achieved?

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What is meant by cleanroom equipment?

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What task do code readers have on a packaging line?

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What are the phases in the lifecycle of the supplier relationship?

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To whom are SOPs addressed?

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When is it imperative to monitor transport temperatures for finished drug products?

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What is industrial hygiene?

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What phases are involved in planning a construction project?

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What is the qualification of a computerised system?

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What are the legal requirements for plastics?

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In which areas should change management be applied and who is responsible for implementation?

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What is meant by measurement chain?

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Which phases are distinguished in the performance qualification of a water supply system?

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What is the European safety referral used for?

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What advantages does quality risk management have for the company?

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What is the minimum requirement for cleaned equipment?

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What is an Establishment Inspection Report (EIR)?

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What elements should be contained in a validation plan for Excel spreadsheets?

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What is the purpose of a responsibility matrix?

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How should raw data be handled?

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What is a root cause?

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How do you determine the frequency of self-inspections?

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What is the verification of a computerised system?

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What are the phases of a qualification of insulated transport boxes?

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Which two aspects of the storage organisation are GMP/GDP critical?

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When is a for-cause audit required?

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What are endotoxins and what are their effects?

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Why must sterile filters not be used in water systems to retain germs?

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How are responsibilities split between Quality Control and Quality Assurance?

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What is the difference between strategic and tactical outsourcing?

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What is the legal status of the European Pharmacopoeia?

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What do the abbreviations VP and VR mean?

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Which sterilisation methods are used in the manufacture of sterile products?

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Where is a qualification according to DIN Spec. 91323 applicable?

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Why has drinking water to be pretreated when using it for pharmaceutical water production?

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What is a Batch Record Review?

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What are responsibilities of the Qualified Person according to EU Annex 16?

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What has to be considered in risk management?

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Which criteria are to be considered when selecting cleaning agents?

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What is the Design Qualification?

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What does quality oversight mean?

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What differences are there between electronic document management systems (eDMS) and electronic quality management systems (eQMS)?

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What is the significance of growth controls in microbiological monitoring?

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Which metrics should be looked at when reviewing the status of a site?

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What is meant by offshoring?

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What is meant by the term 'CAPA' or 'CAPA management'?

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What needs to be considered when validating a sterility test method? | 2024

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What is an informal QRM method?

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What documents are required for operation of a pharmaceutical water system?

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What is required for risk-based decision-making?

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What do inspectors of premises and rooms pay particular attention to?

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What cleaning validation sampling procedures are available for which residues?

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How can subjectivity in the QRM process be minimized?

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What information is required for the registration of any manufacturers, importers and distributors of active substances in the EU?

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Which lubricants can be used in a GMP environment?

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Which parameters are relevant in the monitoring of pharmaceutical water?

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What is a residual risk?

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What is the advantage of a 2D-MatrixCode?

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What are the phases of the quality risk management process?

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What is the required evaluation period for the Product Quality Review?

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What should be done with goods that have been rejected, quarantined or returned from the market?

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What significance do OEBs have?

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What interfaces to other quality systems does the deviation management have?

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Which active ingredient manufacturers receive an EU GMP certificate?

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Is it necessary to wear gloves in cleanroom class D?

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Which role plays a runner during an inspection?

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How can UV irradiation be used in pharmaceutical water generation?

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What is an action limit?

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Which general requirement applies to the design of material locks?

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In which phases is the quality risk management process divided?

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What are the 3 main types of safety features against counterfeit medicines?

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What guidelines and quality standards apply to airfreight?

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What are the so-called safety features on packaging materials?

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What is the difference between cleanroom class and air cleanliness grade?

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Which parameters determine the result of cleaning according to Sinner's circle?

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What is a risk?

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What is an API Starting Material?

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Which different types of stainless steel are available?

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What are the advantages and disadvantages of the swab test for cleaning validation?

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What is the advantage of Building Information Modeling (BIM) for planning new premises?

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What types of impurities may be present in chemical active substances?

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What is meant by active and passive temperature control?

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What are the advantages of integrated qualification?

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What is IT governance?

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What parameters are hidden behind "Feedwater Conductivity Equivalent", and what are they needed for?

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How are self-inspections documented?

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What is a stability commitment?

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What should be considered when selecting a suitable sealing material?

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What is the difference between an EDMS and an EQMS?

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What is the purpose of bulk filling inspection on the packaging line?

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What is the focus for personnel in the revised Annex 1?

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What is a third-party audit?

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What is meant by the term "metadata"?

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How can medicinal products requiring cool transport conditions be transported?

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How is pure steam produced and used?

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What is cloud computing?

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What do typical manufacturing processes look like?

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What is a fishbone diagram used for?

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What are the basic physical principles of steam generation?

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Which criteria shoud be used for the selection of insulated transport boxes?

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What was the reason for the revision of Annex 1?

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What does a challenge-concept for cleaning validation mean?

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What needs to be considered when validating a sterility test method?

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What water quality do you use for cold WFI production?

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What are the requirements for advanced electronic signatures?

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What are the major trends that have changed the concept of validation recently?

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What are the different types of pharmaceutical water?

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Which are the key aspects of personnel hygiene?

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What is important for the processing of deviations?

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How do we deal with risks?

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What is confirmed by an ATP certificate?

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What is DIN Spec. 91323?

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What methods are used for testing leakage?

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What is the Sterility Assurance Level (SAL)?

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What is a generic form?

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What are facility control systems used for?

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What special factors need to be considered for sterile filtration?

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What is confirmed by the written confirmation for imported APIs?

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How can QRM be used?

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What is the FDA inspection report being called?

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Where can you find regulatory requirements for isolator technology?

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What is the Data Lifecycle?

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What do Typical Manufacturing Processes for Sterile Products look like?

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What are the Different Priorities of the Quality Assurance and IT Departments when Operating Computerised Systems?

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Which Quality and Process Parameters must Typically be Taken into Account During Process Validation for Terminally Sterilized Products?

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What are the Prospects and Developments in the Operation of Computerised Systems?

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How can the Specific Requirements for Sterile Products be Taken into Account in the Quality Management System?

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Which Measures are Crucial for Implementation and Monitoring of Data Integrity?

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What is the Importance of Data Integrity?

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What are the Core Tasks of Human Resource Management?

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What Types of Impurities may be Present in Active Substances?


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What are the Phases of a Working Cycle During a Steam Sterilisation Process?

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What are the Basic Principles of Organisational Structures?

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Why is Import Authorisation Necessary for Medicinal Products Entering the EU?

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How do Components like Filling Needles and Laminarisators Affect First Air Integrity?

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How is the Effectiveness of CAPAs Verified?

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How is First Air Verified and Monitored During Aseptic Process Qualification?

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What are the General Requirements for Standard Documents?

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What is the Role of the Logistics Service Provider?

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What are the Benefits and Limitations of Passive Temperature-Controlled Containers for Drug Transport?

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Why is it Important to use Consistent Microbiological Air Monitoring Methods in Pharmaceutical Cleanrooms?

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Who is Qualified to Conduct Self-Inspections within a Company?

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