The drug development process is a long and complex endeavor that involves a wide range of stakeholders, including researchers, scientists, government agencies, and pharmaceutical companies. The process can take many years and is divided into several stages, including discovery, preclinical testing, clinical trials, and regulatory approval. The discovery stage is…
What is a New Chemical entity? A New Chemical Entity (NCE) is a compound that is not identical to any previously approved drug by regulatory agencies such as the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA). These compounds have unique chemical structures that have not…
Behavioral interview questions are a type of interview question that asks the candidate to provide specific examples of how they have handled certain situations in the past. These types of questions are designed to help the interviewer understand how the candidate thinks, reacts, and behaves in different situations, and how…
A Traditional Paper Master File (TMF) is a physical collection of documents that are used to store and manage important information related to a clinical trial. These documents are typically stored in binders or folders and are usually kept in a secure location, such as a study site or sponsor's…
Career goals or resume goals act as the tone of your resume. It spells out your career goals and objectives. This article is in line with the clinical trial candidates and professionals.
The "Protocol" term is derived from the Greek Word “PROTOKOLLON” means a format procedure for carrying out scientific research. A Protocol is defined as the document that describes the background, rationale, objectives, study design, methodology, statistical considerations, and organization of a Clinical Research project. Clinical Research is conducted as per…
Medical writers analyze and interpret medical issues in order to present them as understandable and concise in publications such as health-related magazines, journal manuscripts, regulatory and research-related documents, disease, or drug-related educational and promotional literature. The scientific information in these documents is the science of communicating biomedical data to appropriate target…
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