Home
Use our global calendar of privacy events to locate an event near you.
FILTER BY
Join us for a full problem-based learning experience. This complete one-week certification training gives you the “do’s and don’ts” and the most effective methodology to comply with GDPR requirements and perform effectively the role and tasks of a DPO. he training covers an in depth insight of the GDPR and all implementation obligations; a step-by-step model to put in place the necessary privacy compliant data protection and information security policies in your organisation; guidance in the most cost-effective and efficient ways to comply with the GDPR.
The experienced trainers in the programme follow Maastricht University’s well-known Problem Based Learning methodology: Throughout our training programme you are stimulated to actively work on real-life issues in order to acquire the skills needed to perform most effectively as a DPO in your organisation. Holding the ECPC-B certification from Maastricht University shows employers you are a knowledgeable professional who has acquired the optimal methodology to manage privacy compliance effectively and interact with the rest of your organization in the fast-changing professional environment in which you need to operate.
Get your ECPC-B DPO Certification from Maastricht University!
We are excited to announce that registration is now open to participate in the fifth Annual Summer Course on Privacy Law and Policy organised by the Institute for Information Law (IViR) at the University of Amsterdam (UvA).
The focus of the course is on latest developments in privacy law and policy related to the internet, electronic communications, online and social media. The program will feature a distinguished faculty of European and US academics, regulators and practitioners who will investigate the EU and US legal frameworks and how they operate together.
For questions, please feel free to contact the course organiser Dr. Kristina Irion ([email protected]).
This conference will address how to ensure that the golden age of innovation does not become the dark age of information privacy. Sessions will show how the apparent car crash between innovation and privacy does not need to be a disaster. At one end of the spectrum, innovation can be the enemy of privacy and at the other end, innovation can be an enabler. This conference seeks willingness on both sides to connect with each other in a civilised manner and to find solutions
Conference Series LLC organizing splendorous Pharmaceutical conferences welcomes you to attend the 8th Global Pharmacovigilance & Drug Safety Summit to be held during July 6-8, 2017 in Kuala Lumpur, Malaysia focuses on the advancements in pharmacovigilance and risk management. It is a 3-day event offering the Exhibition, at venue to showcase the new and emerging technologies and have wider sessions involving Keynote presentation, Oral, YRF ( student presentation), poster, e-poster presentations and exhibition.
Global Pharmacovigilance Market is expected to reach USD 5.51 billion by 2020, according to a new study by Grand View Research, Inc. Increasing incidence rates of adverse drug reaction and the introduction of stringent drug safety regulations are some key drivers of this market. ADR is responsible for approximately 5% of the hospitalization in developed countries annually, and this is expected to boost usage rates over the next six years. Pharmacovigilance has witnessed a significant rise in usage rates in the recent times owing to growing global geriatric population triggering a growth in demand for new drug development.
The field of Pharmacovigilance is growing by and large, its development is making high impact in field of Pharmaceuticals and medical sciences. 8th Global Pharmacovigilance & Drug Safety Summit focusses on how the importance and significance can be gauged by the fact that it has made huge advancements over the course of time and is continuing to influence..The main theme of 8th Global Pharmacovigilance & Drug Safety Summit is “Innovations in Pharmacovigilance for Systematic Safety and Management”.
Sessions Include talks on Drug Safety, Adverse Drug Reactions, Pharmacokinetics and Pharmacodynamics, Pre-Clinical and Clinical Trials, Challenges in Pharmacovigilance, Clinical Trials on Various Disorders, Pharmacovigilance Market, Clinical Research and Statistics, Case Report in Clinical Trials, Pharmacovigilance Significance & Scope, Continental Pharmacovigilance, Good Pharmacovigilance Practice, Pharmacovigilance and Risk Management, Medical devices Pharmacovigilance, Veterinary Pharmacovigilance, Biopharmaceutics, PV Data Base Management, PV Consultings And Bussiness opportunity, Regulatory Affairs, Growth strategies in Pharma, Pharmacy Practices and its Challenges
Meet at the experts gathering to Join Global Scientific influencers from , Asia, Middleeast , USA (America), Europe at Pharmacoepidemiology and Clinical Research conferences happening from July 06-08, 2017, Kuala Lumpur, Malaysia. Pharm-epidemiology Congress July 06-08, 2017 at Kaula Lumpur, Malaysia is organised aiming to bring together leading academic professors, scientists, researchers and research scholars to exchange and share their experiences and research results on all aspects of Pharmacoepidemiology and Clinical research. It also provides a premier interdisciplinary pavement for Pharma, Biotech and Medical Device industries and to represent their company and discuss the most recent innovations, trends, and concerns as well as practical challenges encountered and solutions adopted in the fields of Pharmacoepidemiology, Clinical trials and clinical research.
The AI Now Symposium is designed to address the biggest challenges we face as AI moves further into our everyday lives. Leaders from industry, academia, civil society, and government will share ideas for technical design, research and policy directions.
This event is free and open to the public; it will also be live streamed on our website. Learn more about our program and speaker line-up below. (Go to event website for program)
Join us in Santa Clara, CA, July 12–14, 2017, for the Thirteenth Symposium on Usable Privacy and Security (SOUPS 2017). This symposium will bring together an interdisciplinary group of researchers and practitioners in human computer interaction, security, and privacy.
Interested in Participating? The Call for Papers is now available.
The SOUPS 2017 program will also feature a poster session, panels and invited talks, lightning talks and demos, and workshops and tutorials. See all available calls in the Participate section below.
SOUPS 2017 will be co-located with the 2017 USENIX Annual Technical Conference.
Hyatt Regency Santa Clara
5101 Great America Parkway
Santa Clara, CA 95054
Phone: (408) 510-6426
Fax: (408) 510-6449
SOUPS 2017 is co-located with USENIX ATC ’17 and will take place at the Hyatt Regency Santa Clara. USENIX has reserved a block of rooms at discounted rates for conference attendees. Please check back for the rates and how to make your reservation.
Registration: [email protected] or 510.528.8649
Membership: [email protected] or 510.528.8649
Sponsorship: [email protected] or 510.528.8649 x17
Student Grants: [email protected] or 510.528.8649
Proceedings Papers: [email protected] or 510.528.8649 x20
| The EU General Data Protection Regulation (GDPR) is considered a risk-based and accountability regulation. Article 24 (Responsibility of the controller) compels organisations to put in place appropriate technical and organisational measures through policies, procedures and other accountability mechanisms.
Addressing the GDPR accountability obligations early on in your compliance program has significant benefits. Learn to identify existing policies, procedures and other accountability mechanisms that are already providing rules and guidelines for processing personal data in your organisation. Understand how this key step, accomplished early in your GDPR compliance strategy, provides significant benefits by leveraging what is already in place to comply with the GDPR providing the privacy office a running start and early successes. In the webinar, we will also identify how to prioritise creation of new accountability mechanisms to further embed GDPR compliance. Plus, we will show additional benefits such as these accountability mechanisms being repurposed in an Accountability PIA to demonstrate compliance at a project level and repurposed once again to demonstrate compliance at an organizational level. Registration Link: https://register.gotowebinar.com/register/3452361340829179137 |
Please join us at the upcoming Washington, DC KnowledgeNet Chapter meeting and learn about the Federal Government’s Controlled Unclassified Information program. This event will provide an overview of the program’s inception and implementation, and have a discussion about its accompanying National Institute of Standards and Technology (NIST) security requirements for nonfederal entities that handle Federal CUI, which includes government contractors, non-profit organizations, and academic/research institutions.
Speakers:
- Kelley Dempsey, Senior Information Security Specialist, NIST IT Laboratory’s Computer Security Division, National Institute of Standards and Technology, and co-author of NIST Special Publication 800-171
- Mark Riddle, Senior Program Analyst, CUI Oversight and Implementation Lead, National Archives and Records Administration, and co-author of NIST Special Publication 800-171
Moderator:
- Koosh Orandi, Federal Confidential Information Program Lead, US Office of Confidentiality and Privacy, Deloitte Consulting
Thank you to our meeting host, Deloitte LLP, for providing snacks and beverages.
| Register Now |
Registration is REQUIRED. Space is limited.
Workshop Focus
Rapid advances in technology have recently brought the analytics of shared data close to practical, even if the amounts of data are large and the security and privacy requirements stringent. In particular for fields with highly sensitive data such as genomics or other health domains, the wide range of privacy-preserving analytics technologies promise to enable new and exciting applications and scientific breakthroughs.
Though for real-world use, there remain still open questions on necessary and sufficient levels of privacy, regulatory and legal compliance, public acceptance and end-user usability of privacy-preserving algorithms to just name a few.
Workshop Goals
- To take a step back to compare and contrast recent advances in medical analytics.
- To bring stakeholders from Medicine, Law, and Technology together to get a better understanding of the full range of requirements, capabilities, and constraints.
- Discuss the current state of technology and to identify remaining technical and non-technical hurdles for public adaption.
- To identify promising directions for further research and real-world validation approaches.
The workshop will not publish proceedings: The goal is to share and summarize progress and insights so far in a conference report that will be published. Furthermore, speakers will be free to publish their talks and any accompanying material online.