Data analytics in Healthcare can prove to be a boon for hospitals and health systems, if used the right way. In addition to focusing on facts, understanding the analytics discoveries can benefit healthcare institutions greatly by improving the management and quality of care. In the process of providing healthcare, institutions collect and store a large amount of patient data that includesinformation of admission, diagnosis, treatment and discharge. Analyzing such data can lead to improved care. Big data is taking every industry by storm and healthcare is no exception. Although a number of organizations have already begun making use of the big data, others need to implement the right infrastructure to generate useful insights. Let’s have a look at how the healthcare organizations can turn big data into strategic assets to deal more effectively with the ongoing challenges, improve operational efficiency and increase profitability.
Food safety is an important concern in food industry. And, if you work in a food processing facility, you always need to be audit ready. With time, food audits have become more and more rigorous and frequent. There are different types of inspections for which it’s important that you have appropriate systems in place. At times, food audits can be overwhelming and challenging as there are numerous regulations and requests which become difficult to comply with. However being prepared for a food safety audit gives you an edge and helps you gain a good audit score which contributes to the business success.
Social media has a profound impact on every aspect of our lives be it communication, travel or healthcare. Every industry is making use of social media, in some way or other and healthcare is no exception. Mobile phones and applications play a crucial role in our lives by allowing people to research symptoms, medications, doctors etc. Social media has become a major tool for sharing healthcare related information, including opinions on different therapies, reviews about doctors, people’s experiences with illness and many more. Internet provides plethora of health related information at our fingertips and many of that information is consumed through social media.
Impact of Social Media on Healthcare Providers
Healthcare providers are significantly benefitted by the social media. It helps them not only in social networking but also in patient education and information sharing. A number of practitioners have claimed that social media usage has helped them in their career advancement and staying updated about the latest findings and information. However, there are a few hindrances in this aspect too which include time requirements, employer backlash, fear of saying something wrong, and being unversed with the technology. Still social media is perceived as a tool for getting low-cost health information and as an opportunity to reach out to relevant communities. Some of the providers have also claimed that social media helps them improve the quality of healthcare. However, for healthcare providers too, social media is not risk free. Indulgence in social media should be in compliance with HIPAA regulations. Also, there could be legal as well as ethical issues for the usage of social media by healthcare providers.
Providing good healthcare services requires a good coordination among a number of people and organization that work together to maintain the quality as well as compliance in the services. No healthcare organization can work alone, be it a hospital, clinic, long-term care company or a dental practice, and it has to rely on vendors or third parties for its functioning. However for every healthcare organization, it is important to know and monitor the company it is partnering or working with to ensure that compliance and quality are being maintained. With time the federal and state regulations are growing more and more complex which is also increasing the risk of regulatory violations. This calls for a heightened need of ensuring vendor compliance for healthcare organizations.
Talking of product safety, the goods that require maximum scrutiny are health, food and beauty products. To make sure that the suppliers and manufacturers belonging to this sector are maintaining the standards set by government agencies, GMP audits are necessary. It’s important to ensure that the manufacturing process is well defined and controlled and the product matches the predefined specifications. In case alterations in the procedures affect the product, there must be appropriate procedure for analyzing the product for its quality. And, if the quality gets compromised, the product must be discarded. Customers should receive the product with clear and understandable instructions. GMP audits ensure that all the procedures in the supply and manufacturing units are in accordance with the recommended practices and the products meet the quality specifications.
Quality control is an extremely important aspect of food industry. This industry deals with very sensitive products and it’s necessary to maintain quality standards and comply with various regulations. In case of food products, most of the people tend to stick to the same brand which matches their expectations and are perceived as of good quality. Companies in food industry need to be very careful as even a small instance of quality compromise could bring them bad reputation and ruin their image. Thus, following the proper procedures in various stages of quality control in food industry is very important if you want to establish yourself as a good and reliable brand. Quality control aims at identifying and correcting the defects in finished products. It is done by identifying the source of the problem and eliminating it to achieve the expected quality standards. Quality control involves regular inspection of quality management and there is usually a specific team which takes care of it.
Every organization needs high potential employees to achieve goals and make profits. And, it’s extremely important that those employees stick to the organization and contribute effectively. Employee retention is one of the most important yet most overlooked aspects in many companies. Research suggests that retaining top talents in your organization could be the key to sales growth, high morale and satisfied customers. On the other hand, loosing important employees leads to reduced productivity and it could also cost the company more than the employee’s salary, in the process of finding a new and good employee. There are a number of factors that lead to employee turnover such as lack of opportunities, ineffective management, lack of appreciation, work pressure and more. This calls for effective employee retention strategies aimed at providing a superior work experience to your employees.
A Standard Operating Procedure (SOP) is defined as a written instruction that elaborates how a task should be performed including when, by whom and where. SOP plays a crucial role in ensuring consistent quality in the pharmaceutical products and best practices in the pharmaceutical unit. It also plays a major role in risk mitigation and therefore proper implementation of SOP is essential. Creating and maintaining SOPs could be a complex task. And, most of the SOPs are quite complicated to read and follow on a daily basis. They mostly contain too much of details and instructions which often increases the risk of errors. Writing effective SOPs for pharmaceuticals is all about documenting the right amount of details that help in carrying out a quality procedure without causing confusions. Many companies write SOPs that emphasize “how” but do not essentially cover “why.”
FDA audit could be nerve-racking for medical device manufacturers if they are not well prepared. Over the last few years, medical device firms have encountered a significantly heightened number of inspections that resulted in increase in the number of citations. Although difficult, FDA audit is an important aspect of medical device industry. However, especially for startups, the first audit could be quite difficult to handle as the checklist of FDA could scare away the potential investors or customers, hindering the organization’s goal and efforts. Moreover, FDA sometimes announces their audit beforehand but the regulators may also turn up any time for inspection, without any notice. This implies, being a medical device manufacturer, you always need to be prepared for going through an FDA audit.
Getting accurate results in clinical trials depends on several factors and an important one among those is site selection. For executing a clinical trial successfully, it’s important to identify and work in an effective site that ensures that the patients are safe and the procedures are effective. While selecting a site for clinical trials, several things need to be considered like availability of suitable patients, experienced staff, track record with previous trials, diagnostic and therapeutic equipment available, geographic location etc. The sponsor needs to perform due diligence to make sure that the site meets all the requirements for the successful execution of a clinical trial. Budget of the trialalso needs careful consideration in site selection for clinical trials. Continue reading “Site Selection for Clinical Trials – Best Practices”