Webinars & Events

WEBINAR

Regulatory compliance is a moving target, and there is no one way for companies to protect their brand, business, market access and human resources from risk.

WEBINAR

Companies in scope of the European Union (EU) Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) Regulation have new requirements under the EU Waste Framework Directive (WFD). Meanwhile, the January 5, 2021, deadline for submitting Substances of Very High Concern (SVHC) data to the Substances of Concern In Products (SCIP) database is fast approaching, and amendments to the EU Medical Device Regulation (MDR) have created additional data management challenges.

WEBINAR

As a best-selling author, photographer and law counsel, Hugh Brown’s work building transparency into the global artisanal and small-scale mining (ASM) industry has taken him to some harsh, remote locations. Along the way, he’s developed an impartial, bird’s-eye view of the sector.

WEBINAR

To manage new European Union (EU) Waste Framework Directive (WFD) requirements effectively, companies need swift, digital access to supply chain data. Join subject matter experts from Assent Compliance and PTC as they discuss how their integrated platform technologies can keep your product compliance data up-to-date and synced with the Substances of Concern In Products (SCIP) database, helping you maintain access to the EU selling region.

WEBINAR

The business environment changes constantly, and the COVID-19 virus is a sobering example of the extreme disruption these changes can cause. Like the ecosystem you operate in, your suppliers’ ecosystems are impacted by the pandemic, increasing your risk.

WEBINAR

The Democratic Republic of the Congo (DRC) is the world’s largest cobalt supplier, but many of the region’s artisanal and small-scale mining (ASM) operations are controlled by armed groups and use child labor. To mitigate supply chain risks, companies are avoiding cobalt purchased from independent miners — a reaction that may cause more harm than good to both the region and industry.

WEBINAR

To meet new requirements under the European Union (EU) Medical Device Regulation (MDR), companies are engaging their suppliers for up-to-date information and reevaluating product composition. Join Travis Miller, Assent’s General Counsel, and Marc Fowler, PTC’s PLM Life Science Sales Leader, as they discuss how the PTC and Assent platforms work cohesively to acquire accurate, quality data that stands up to external scrutiny from regulatory and notified bodies.

WEBINAR

Your suppliers, customers, distributors and other partners present a multitude of risks to your business. While you can save time by screening these third parties through databases, it is not a substitute for comprehensive due diligence.