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May 1, 2022
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May 5, 2022(1 event)
12:00 pm: How to Proactively Predict & Mitigate Risk Throughout the Supply Chain12:00 pm: How to Proactively Predict & Mitigate Risk Throughout the Supply Chain – If any of your supply chain falters, use unethical employment practices, have unhealthy or hazardous working conditions, produce unsafe products, operate environmentally-unsound production plants, your organization’s reputation could be seriously compromised. You’ll be given creative and cost conscious solutions to identify risks, prioritizing the highest risks, assigning responsibility to the appropriate risk owners, mitigating risks (containment, control, prevention) & communicating with stakeholders (both internal and external, including regulatory agencies). |
May 6, 2022
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May 21, 2022
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May 24, 2022
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May 25, 2022(1 event)
11:00 am: Using STEP And SciLeads To Grow Your Texas BIOTECH Business11:00 am: Using STEP And SciLeads To Grow Your Texas BIOTECH Business – Join the live webinar with Laura Haldane as she introduces SciLeads, an innovative life science and applied research lead generation platform. SciLeads works with bioscience companies in Oregon and around the world to accelerate their sales by enabling them to quickly find and engage with targeted and funded leads, and develop outreach strategies. |
May 26, 2022
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May 29, 2022
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May 30, 2022
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May 31, 2022
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June 1, 2022
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June 2, 2022(1 event)
12:00 pm: How to Survive an FDA Inspection12:00 pm: How to Survive an FDA Inspection – A big challenge with all medical device manufacturers is to be compliant with any regulations applicable with their product. In the case of the United States it will include 21 CFR Part 820 which is a set of regulations from the FDA that outlines the current good manufacturing practice (CGMP) requirements that manufacturers must follow with regards to their quality system. Register for this free webinar where Anne Holland, CEO of QA Consulting with 20+ years experience advising medical device companies on regulatory and quality needs, will share some preventative actions that your medical device company can take to minimize the possibility of receiving a 483 which in some cases could result in a product seizure. |
June 3, 2022
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June 4, 2022
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