One of the biggest challenges of running a business is the sheer number of regulations that must be followed to bring your service or product to market. Paperwork and reporting requirements using the wrong QMS can make quality management difficult and costly. Requirements can vary by a multitude of factors, such as region, consumer demands, […]
Equipment maintenance and management of assets can be a small added cost to your business compared to the huge loss that can occur during a breakdown. Thus, it is important for Isolocity to always continue improving equipment protocol to make it easier for you to get even more effective equipment maintenance, without extra work. In […]
Change control procedures are crucial to the success of business operations since they help reduce the amount of unnecessary change or disruptions caused by inefficient processes. Thus, Isolocity has added more flexibility and control for operators that require additional classification and scope of impact to make more meaningful decisions – while making it easier to […]
The global supply chain has become more complex. As companies seeking to maximize the value of their products find ways to collaborate with others across the globe. Even the short time that it spends at one processing stage could mean multiple touchpoints with multiple people or departments. Thus, it is not surprising that consumers and […]
The sale of cannabis has seen a boost through its legalization for medical purposes. For most growers, it’s meant a change in how they work from seed to sale. Now there are compliance and quality control regulations that businesses in the cannabis industry must follow. Finding the best way to manage your cannabis business is […]
Change control is a crucial part of the product or service management process. They help avoid any unnecessary changes that could disrupt business success and ensure that resources are used efficiently. With the size and structure of an organization becoming ever more complex, it is important for such measures to be flexible to fit the […]
Delivering a product or service today often involves the collaboration of multiple teams, applications and infrastructure. With the growth of cloud computing and automation technology, it isn’t a surprise that workers are increasingly switching between 10 or more applications a day in order to complete their tasks. This ultimately creates an environment where disjointed communication, […]
The Medical Device Single Audit Program (MDSAP), enables auditing organizations recognized by the MDSAP to conduct one regulatory audit or medical device manufacturers that satisfies the requirements associated with the participating authorities of the program.
Companies that are committed to quality are always looking for ways to improve. When a process is running smoothly, they explore new ways of enhancing workflow. When something breaks down, they take extra steps to ensure a clear
The global vaping market is expected to grow to a worth of over $29 billion by 2022. As with any lucrative but potentially risky market, there are several FDA regulations in place and GMP is crucial to producing quality products. In fact, because of the rigorous Premarket Tobacco Product Applications process, or PMTA, exercising GMP from the […]
Finding ways to optimize quality control is important. In fact, it should be one of the top priorities of all high-performing companies. Even the smallest companies are now competing against big corporations. Therefore, ensuring that one’s products are always of optimal quality is imperative to the overall success of your company. Consumers have to be […]
Isolocity is proud to announce that we have partnered with the Canadian Vape Association (CVA) to develop the GMP e-liquid vaping standard guidelines, and will be presenting them to Health Canada and the rest of the industry. Our co-founder Chris Budd will chair the CVA standards committee with the help of other Canadian industry subject […]
Join us at our next cannabis event in Toronto, at the Metro Toronto Convention Center! Lift & Co. Cannabis Expo is a yearly event where businesses in the industry gather to network and share knowledge.
Join us for our next cannabis event presentation at the Canadian Cannabis Summit 2019. Our presentation “Why GMP? Understanding Compliance in the Cannabis Open Market” will break down these topics and more.
On May 2016, the US Food and Drug Administration (FDA) decided that electronic nicotine delivery systems (ENDS) companies must follow the same rules as tobacco products. It includes:
Join us for our next vape event presentation at Next Generation Nicotine Delivery USA 2019. Our presentation “Why GMP? A Case Study On Automating Compliance For Vape” will break down these topics and more:
GMP stands for Good Manufacturing Practices, it is a compliance standard in production and manufacturing industries. GMP guidelines are aimed at making the production line more consistent and aims to give better control
HACCP or Hazard Analysis and Critical Control Points is a process by which food and beverage makers can limit the amount of biological, chemical, and physical hazards that can harm finished products. It is an approach that prevents and helps
The burgeoning vape industry is about to transform side by side with its exponential rise. As with any new emerging industry, there are always regulations that need to be updated or created in order to better serve its community and the public.
Quality management is a resource-intensive business activity. When implemented properly, it offers a significant return on investment. Many companies that rely on production equipment to manufacture goods have selected the
How to Implement 5S In The Workplace Your company’s production and efficiency is dependent on the organization of your work spaces. Cluttered spaces create risks for employee mistakes, bottlenecks, worker safety, and worker morale. Leaders look to methods such as 5S in the workplace
