12:00 pm: How to Proactively Predict & Mitigate Risk Throughout the Supply Chain
12:00 pm – 1:00 pm May 5, 2022
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).
9:00 am: NAMSA Training Series: ISO 10993-18:2020 Chemical Characterization of Materials
9:00 am – 3:45 pm May 19, 2022
In this session, NAMSA will discuss the chemical characterization of materials and the evaluation steps to choose proper tests, extracts and test durations to meet the latest industry requirements. This workshop will include instruction and multiple hands-on exercises guided by an experienced NAMSA instructor.
11:00 am: Using STEP And SciLeads To Grow Your Texas BIOTECH Business
11:00 am – 11:30 am May 25, 2022
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.
Also joining Laura is Logan Banfield from Texas Department of Agriculture who will speak about how the STEP grant program can contribute toward the cost of the SciLeads database subscription.
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.