Physicians and healthcare professionals understand the importance of providing effective medications to their patients. To provide the highest standard of healthcare and prescribe quality medications, they must trust pharmaceutical companies to produce effective products. Pharmaceutical companies must be able to rely on their research and development teams to create and test effective medications that can be used in the treatment of illness and disease. Quack medications have no scientific evidence to back up their claims and often leave customers in worse condition than when they started.
Testing and Clinical Trials
From the laboratory technicians to the nurses who monitor patients participating medical trials, pharmaceutical companies meticulously formulate, test and document everything they can when researching the possibilities of a new medication. The accuracy of their clinical trials and testing procedures ensure both the safety and effectiveness of each medication or technique they develop.
Pharmaceutical companies are required to follow specific protocols and guidelines during the testing of the medications they produce. This ensures accurate results and provides substantiated proof that a medication fulfills the claims of the manufacturer.
Guidelines and Restrictions
The FDA (Food and Drug Administration) has put in place specific rules and regulations that must be followed by pharmaceutical companies. Pharmaceutical quality assurance teams are required to take every precaution to ensure all guidelines and restrictions are explicitly followed. Temperature, humidity and air quality are constantly monitored to ensure a neutral environment during the development and production processes.
Companies who do not follow federal regulations and test their medications run the risk of introducing quack medications that are unreliable and ineffective. Without proper pharmaceutical quality control measures, companies have no way of verifying the claims they make concerning their medications. Untested medications can often worsen a patient's symptoms and prolong their illness.
FDA Approval
The FDA approves medications which have passed through all of the restrictions and protocols that have been put in place to assure their safety and effectiveness. Each medication approved for public use must pass through 7 years of trials and testing protocols. Companies who do not follow these standards cannot claim to be FDA approved.
Customer Satisfaction
The pharmaceutical quality assurance and control standards pharmaceutical companies use are in place to protect the rights and health of the consumer. Most companies feel it is important to do everything possible to produce a high quality product. Companies that produce quack medications only strive to draw the public in with false claims and promises in the hopes of gaining customers.
Consumers have the right to file personal injury claims against companies who sell products that are falsely labeled or have caused them harm. Taking an untested medication that causes or worsens existing health conditions can create additional health concerns. Reporting quack medications to the FDA is the first step in getting them removed from the shelves and prevent others from being harmed.
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Valeria Stephens is a Copywriter at Higher Education Marketing, a leading Web marketing firm specializing in Google Analytics, Education Lead Generation, Search Engine Optimization (SEO), Mobile SMS Alerts, Social Media Marketing and Pay Per Click Marketing, among other web marketing services and tools.
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