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November 2020

SCCE Virtual Nonprofit Sector Compliance Conference

November 5 @ 9:20 am - 3:30 pm CST
$175 – $195

This full day virtual conference held on November 5 is dedicated to managing and understanding the unique and significant compliance issues faced by nonprofit organizations. The charitable organization sector faces many compliance challenges, including unique tax exemption issues, fundraising registration and related issues, privacy and data security, complex reporting requirements, and many more. Nonprofit organizations also find themselves vulnerable to unique fraud and conflict of interest concerns. This conference will be in Central Standard Time (CST).

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The True ROI of Automated Data Privacy Compliance

November 5 @ 12:00 pm - 12:45 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
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Free

Data privacy regulations have become even more onerous since the GDPR was enacted in 2018, with new obligations in multiple jurisdictions (like the LGPD in Brazil) and proposed changes to the CCPA on the ballot for November. In addition, budgets and headcount are still strained as a result of the pandemic. Furthermore, the costs of a data breach to a company's bottom line and reputation could be insurmountable. But data privacy compliance does not have to break the bank. In…

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The True ROI of Automated Data Privacy Compliance

November 5 @ 12:00 pm - 12:45 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
+ Google Map
Free

Data privacy regulations have become even more onerous since the GDPR was enacted in 2018, with new obligations in multiple jurisdictions (like the LGPD in Brazil) and proposed changes to the CCPA on the ballot for November. In addition, budgets and headcount are still strained as a result of the pandemic. Furthermore, the costs of a data breach to a company's bottom line and reputation could be insurmountable. But data privacy compliance does not have to break the bank. In…

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Essentials of Compliance Investigations Conference

November 9 - November 10
$499
Online Event

This virtual conference takes place in Central Standard Time (CST) Learn the core principles of conducting effective compliance investigations so that you're prepared next time you are called upon. Receive detailed and valuable information from experienced investigators: Meric Bloch and Albert Gagne. Topic include: Investigation Basics Planning the Investigation Gathering Evidence & Documentation Conducting Interviews Reporting Results After the Investigation The First Information is Almost always wrong Registration includes a free 12 month digital subscription to Meric Block's book: The…

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SCCE Essentials of Compliance Investigations Conference

November 9 @ 10:00 am - November 10 @ 2:00 pm CST
$379 – $499
Online Event

Attend SCCE's virtual Essentials of Compliance Investigations Conference November 9-10, 2020. The event will take place in Central Standard Time (CST). Learn the core principles of conducting effective compliance investigations so that you're prepared next time you are called upon. Receive detailed and valuable information from experienced investigators: Meric Bloch and Albert Gagne. Topic include: Investigation Basics Planning the Investigation Gathering Evidence & Documentation Conducting Interviews Reporting Results After the Investigation

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6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

November 11 @ 8:00 am - 2:00 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
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$545.00

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues.

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6-Hour Virtual Seminar on The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities

November 11 @ 8:00 am - 2:00 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
+ Google Map
$545.00

This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together. Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues. Part of these arrangements typically involve the development, support and updating of…

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ACES Summit

November 12 @ 10:15 am - November 13 @ 2:15 pm UTC-5
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
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Free

Connect with and learn about the latest challenges and strategies from leaders in the industry and fellow in-house legal experts and compliance officers. We build in plenty of networking time so you can build the business relationships that are key to success. Registration is only open to in-house and corporate counsel and executives.

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HCCA’s 2020 Healthcare Enforcement Compliance Conference

November 15 - November 18

Regulations play a major role in the health care industry and it can be overwhelming to understand and stay on top of everything. This conference is a once-a-year opportunity to gain insight into properly monitoring, detecting, investigating, and managing violations. You will hear directly from government officials and the unique perspectives of those who deal with regulations daily. Connect with other healthcare compliance professionals, earn CEUs, take advantage of the opportunity to sit for the Certified in Healthcare Compliance (CHC)® exam…

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SCCE Basic Compliance & Ethics Academy

November 16 @ 8:00 am - November 19 @ 4:00 pm EST
$2750 – $3250

Attend SCCE Basic Compliance & Ethics Academy in Fort Lauferdale, FL November 16-19, 2020. Our Basic Academies are ideal for professionals with some compliance knowledge and experience who are ready to support, enhance and manage a comprehensive compliance program.  They are taught by compliance professionals, hand-selected for their experience and teaching skills. Topics include compliance policies and procedures, education and training, risk assessment, auditing and monitoring, conflicts of interest, and anti-corruption and bribery. Course materials are provided onsite on the…

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6-Hour Virtual Seminar on Applying ISO14971 and IEC62304 – A guide to practical Risk Management

November 16 @ 8:00 am - 2:00 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
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$545.00

Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Most activities cannot be retroactively performed since they are closely linked into the development lifecycle. Diligent, complete and correct implementation of risk management from the start of product development is therefore imperative. This course will introduce all necessary steps to design, implement and test critical medical devices in a regulatory compliant environment. This course will additionally address the software risk management and…

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6-Hour Virtual Seminar on eCTD Submissions of IND/NDA to the US FDA, EU and Canada

November 16 @ 8:00 am - 2:00 pm CST
Online, Compliance Key,364 E Main Street, Suite 1009
Middletown, DE 19709 United States
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$545.00

The international agreement to assemble all Quality, Safety and Efficacy information for a drug or biologic product into a common format (called the CTD - Common Technical Document) has improved the speed and efficiency for companies working in global development programs and clarified expectations by regulatory bodies. Reformatting for multiple submissions is substantially limited.  The CTD has improved the regulatory review processes and enabled implementation of good review practices. The eCTD has increased efficiency for reviewers and improved submission times. …

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