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From Lab to Pharmacy: The Reality of Bringing a Drug to Market

Author Name: Boutika Profession: clinical Research Introduction: Drugs are chemical agents that alter the physiological or psychological functions of living organisms. They are used in various ways, such as for diagnosis, treatment, and prevention of diseases, or to promote well-being. Read more: telemedicine and its potential for healthcare access Drug discovery is a massive process that leads to the development or introduction of a new molecule into the market for the benefit of society. It takes around 12–15 years for a drug molecule to be fully established as a new drug candidate. Just imagine the expenditure required to finally bring it to market. It takes more than $1 billion to carry out this drug discovery process. Process: The process of drug discovery involves several key steps, which include:  Pre discovery  Pre clinical research  Clinical research  Regulatory approval process  Post-Marketing Surveillance Now, let's learn about them one by one. Pre di...

The Pill's Journey: Understanding the Role of Drug Formulation

Author Name: Boutika Profession: clinical Research Introduction Drug formulation involves designing and developing a pharmaceutical product by blending the active pharmaceutical ingredient (API) with appropriate excipients. These excipients play a vital role in maintaining the drug’s stability, optimizing its effectiveness, and improving patient compliance. The formulation process is essential in defining how the drug is delivered, absorbed, and utilized by the body. Read more: From lab to pharmacy: Reality of bringing a drug to the market The significance of drug formulation extends beyond simply mixing ingredients—it ensures: Stability throughout its shelf life Effective delivery of the API to the target site Compliance with safety and regulatory standards Enhanced patient adherence through optimized dosage forms Purpose of Formulation in Drug Development The primary goal of drug formulation in development is to convert a drug candidate into a safe, effective, and manufac...

Contract Research Organization (CRO)

A Contract Research Organization (CRO) is a specialized service provider that supports pharmaceutical, biotechnology, and medical device companies in conducting clinical trials and research. CROs play a crucial role in bringing new drugs and therapies to market by managing various aspects of the clinical trial process, from protocol development to regulatory submissions. They act as a bridge between sponsors and regulatory authorities, ensuring compliance with stringent guidelines. CROs offer both expertise and infrastructure to manage clinical trials efficiently, reducing the burden on sponsors and allowing them to focus on core activities like drug development and innovation. Why Choose a CRO for Clinical Trials? Collaborating with a CRO offers numerous advantages, including: Expertise: CROs bring extensive knowledge of regulatory requirements and clinical trial processes, ensuring trials meet the highest standards. Cost-Effective Solutions: By outsourcing research activities, sponso...

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Our website aims to bridge the gap between industry professionals, job seekers, and students who are interested in learning about the clinical trial process and the critical role that play in advancing medical research. Our Mission is to provide accurate, up-to-date, and actionable insights into the clinical trial industry, empowering both individuals and organizations to make informed decisions about their involvement in medical research. Whether you're a healthcare professional, a job seeker looking to start a career in clinical research, or a pharmaceutical company searching for a reliable CRO partner, our website has something valuable for you.

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