• How to Choose the Best QMS

    Posted August 26th, 2021 By Maria Lam

    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, […]

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  • Enhanced Equipment Maintenance & Updated Workflow

    Posted June 19th, 2021 By Maria Lam

    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 […]

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  • Scope of Impact, Classification & Action Items For Change Control

    Posted April 22nd, 2021 By Maria Lam

    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 […]

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  • Enhanced Product Traceability with Audit Trails / Activity Tracking

    Posted March 15th, 2021 By Maria Lam

    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 […]

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  • QMS & Seed-to-Sale: How Each Can Benefit Your System

    Posted February 26th, 2021 By Maria Lam

    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 […]

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  • Flexible Document Change Control & CAPA Management

    Posted January 12th, 2021 By Maria Lam

    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 […]

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  • Connect Distributed Teams With Multilingual Support & Okta

    Posted December 31st, 2020 By Maria Lam

    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, […]

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  • Improving MDSAP Audit Efforts with Automation

    Posted November 30th, 2020 By Maria Lam

    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.

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  • Improving Organizational Efficiency With 3×5 Why Analysis

    Posted August 11th, 2020 By Maria Lam

    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

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  • All About the PMTA Deadline (Premarket Tobacco Product Application)

    Posted August 3rd, 2020 By Maria Lam

    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 […]

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  • Remotely Managing Risks With PFMEA

    Posted May 13th, 2020 By Maria Lam

    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 […]

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  • Isolocity Co-founder To Chair Vaping Standards Committee

    Posted September 5th, 2019 By Maria Lam

    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 […]

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  • Lift & Co. Cannabis Expo 2019

    Posted May 31st, 2019 By Maria Lam

    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.

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  • Canadian Cannabis Summit 2019

    Posted May 18th, 2019 By Maria Lam

    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.

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  • All About FDA 21 CFR Part 11

    Posted May 6th, 2019 By Maria Lam

    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:

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  • Next Generation Nicotine USA 2019

    Posted April 26th, 2019 By Maria Lam

    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:

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  • What Are The GMP Guidelines?

    Posted August 1st, 2018 By Maria Lam

    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

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  • What is HACCP?

    Posted May 24th, 2018 By Maria Lam

    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

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  • What You Need to Know About Bill S-5

    Posted April 20th, 2018 By Maria Lam

    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.

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  • Improve Productivity With TPM Implementation and OEE

    Posted December 18th, 2017 By amlorriman

    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

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  • 5S In The Workplace

    Posted August 22nd, 2017 By amlorriman

    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

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