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Preparing for an Inspection or Accreditation Survey – Part 2

National Association of Boards of Pharmacy

Then, walk through each step of the practice of pharmacy such as data entry; drug utilization review; compounding; final association between the drug, the prescription, and the label (eg, the dispensing act); and patient counseling.

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Data integrity considerations in Pharma and Life Sciences

European Pharmaceutical Review

Transparent communication with regulatory authorities ; this is key during the product development and regulatory submission process. It is advisable to address any concerns or issues related to data integrity proactively and demonstrate a commitment to resolving them in a timely and effective manner.

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How using AI in clinical trials accelerates drug development

Pharmaceutical Technology

Once the target is identified, researchers work to develop a compound that can interact with it. After a promising compound has been identified, it’s tested in preclinical models to evaluate its safety and efficacy. AI also helps in interactions with patients, as it can be used for automating patient recruitment and data collection.

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How to perform operational qualification – step by step

GMPSOP

The data entry and retrieval process, user access and security, electronic signature, audit trail, system integration, performance, printing, etc. – Gas Chromatography (GC) Systems (Critical for analyzing volatile compounds). Also, it can be integrated with other external interfaces. are functioning as expected.