October 12, 2021
Clinical Trial Manufacture
Clinical Trial Manufacture This story and thinking behind that statement can be traced back to war crimes. During the Second World War, the Nuremberg Code was the most influential and widely quoted code, which originated in the so-called medical research carried out in the concentration camps. Part of the judgment at the “Doctors’ trial” at…
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October 5, 2021
Overview Of EU Law
Overview of EU law Europe as a society and union The European Union as an institution is neither a State nor an organisation. It is a union of states based on the rule of law and democracy. Each Member State delegates sovereignty over specific activities to common institutions that represent the interests of the Union…
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September 29, 2021
Pharmaceutical Law and Administration
Pharmaceutical Law and Administration Medicine Laws have been introduced around the world to protect the patient. Many of these were the result of disasters that caused harm to patients. Two examples of this were the following: USA 1937 – Sulphanilamide Tragedy, where over 100 children died when a company sold a syrup of sulphanilamide that included…
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June 30, 2021
Coronavirus Impact on the Tourism Industry Worldwide
Coronavirus Impact on the Tourism Industry Worldwide The coronavirus pandemic has had a profound impact on the global tourism industry. Here is a summary of its effects: Travel Restrictions: Governments implemented strict travel restrictions, including border closures and mandatory quarantines, which severely limited international and domestic travel. These measures resulted in a significant decline in…
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June 29, 2021
Design of an Efficient Stability Programme -Bracketing and Matrixing
Design of an Efficient Stability Programme -Bracketing and Matrixing Design of an Efficient Stability An efficient stability program is essential for assessing the quality and shelf life of pharmaceutical products. Bracketing and matrixing are two strategies commonly used to design such programs. Bracketing involves testing representative samples, such as the highest and lowest strengths, at…
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June 29, 2021
QP Declaration
QP Declaration Qualified Person (QP) declaration A Qualified Person (QP) declaration is a critical aspect of the pharmaceutical industry’s quality assurance process. In the European Union (EU), a QP is responsible for ensuring that each batch of medicinal product complies with regulatory requirements before it is released for sale or distribution. Here’s a brief overview…
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June 27, 2021
NHS study finds that CT scan gets 70% of Lung Cancer
NHS study finds that CT scan gets 70% of Lung Cancer A significant NHS study has found that a massive number of lives could be saved if individuals at risk of developing Britain’s deadliest cancer were screened to detect it before it becomes serious. Around 48,000 individuals a year are determined to have the infection…
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June 27, 2021
How to Apply DQ/IQ/OQ/PQ in New Framework
How to Apply DQ/IQ/OQ/PQ in the New Framework Apply DQ/IQ/OQ/PQ DQ/IQ/OQ/PQ, also known as Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), are essential components of the validation process in various industries. Here’s a brief overview of how to apply them in a new framework: Design Qualification (DQ): DQ focuses…
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June 14, 2021
Overview of the HACCP System
Overview of the HACCP System Hazard Analysis Critical Control Point (HACCP) is a system that identifies, evaluates, and controls food safety hazards. This system was developed by the pharmaceutical industry to help ensure that food products are safe for consumption. The HACCP system is a preventative approach to food safety, as it focuses on preventing…
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