GDPR Services

We provide a range of services from fully GDPR outsourced services
to cut to fit GDPR compliance solutions for the most innovative science.

EU Data Protection Representative

Businesses situated outside the European Economic Area (EEA) must adhere to the data processing regulation by mandating the appointment of a data protection representative (DPR) as a non-negotiable obligation. iliomad, leveraging its European presence via regional offices, steps into the role of the European Data Representative for instances when the data of EU citizens undergoes processing. This designated natural person not only acts as the primary liaison for supervisory authorities but also embodies a critical safeguard detailed in the Informed Consent Form (ICF), a standard protocol particularly in the context of clinical trials. The DPR's duties involve ensuring compliance with protection and privacy mandates, overseeing processors, and contributing to privacy by design. They are instrumental in implementing protection rules, managing impact assessments, and instituting precautions against breaches. Furthermore, this role carries the responsibility to ensure that the processes in place are compliant, thus mitigating the risk of penalties while upholding the stringent obligations of data protection and privacy.

EU Data Protection Officer

Appointing a DPO is a mandatory step for a number of companies operating in medical research. Iliomad can act as your external DPO and establish your company’s compliance system.

Data Protection Impact Assessments

Iliomad’s expertise in conducting DPIAs for medical research can help you speed up your compliance program as well as benefit from iliomad’s unique templates and methodology.

Start assessing!

Due Diligence

iIliomad can assist you in thoroughly addressing all privacy-related requirements, ensuring that every necessary step has been taken to safeguard data. In the event of any privacy shortcomings, we can develop a detailed remediation plan to rectify these issues. Our expertise can play a vital role in securing a successful financing round and instilling confidence in your prospective financial partners.

Data Privacy Training

Mandatory GDPR training for all personnel involved in the processing of EU personal data is essential. Ensuring a consistent level of data protection across the entire company, from operational staff to management teams, is of utmost importance.

Train your team

Clinical Data Hosting

Hosting of clinical data has become a major concern for companies processing EU personal data. Iliomad can help you establish your hosting strategy and become compliant with hosting regulations

GDPR Quality Assurance

iliomad has crafted a bespoke and adaptable GDPR Quality Assurance (QA) system specifically designed for Life Sciences companies. This system is scalable, making it a suitable solution for everything from small biotech startups to large pharmaceutical corporations

In need of QA assistance?

Informed Consent Form Review

Informed Consent Forms are pivotal documents for clinical trials and privacy is now at the center of those documents. With its broad experience in the EU, iliomad can help speed up the process.

Let's be in touch!

GDPR Contractual Review

Iliomad has developed a broad experience within the life science industry to help every party abide with the GDPR and tackle the numerous correlated constraints.

Vendor Assessment

Vendors processing activities ranging from hosting patient data to data analysis must also comply with data privacy regulations. Iliomad can help you assess your vendors capabilities and measures to make sure your data is in good hands.

Gap Analysis: UK GDPR, HIPAA, PIPEDA & PIPL

We help our clients through gap analysis with the GDPR and other main privacy regulations. Iliomad has developed extensive expertise of the main privacy regulations of the world and can help you.

European Local Regulations

The General Data Protection Regulation (GDPR) is a regulation that aims to provide a consistent set of data protection rules across the European Union (EU). Although the GDPR is a European regulation, it allows EU member states to adapt certain provisions to better align with their national laws and practices. This can lead to nuances and variations in the way the rules are applied. Additionally each EU member state has its own regulator responsible for enforcing the GDPR. These authorities may have slightly different interpretations and different enforcement priorities.

UK Data Protection Act

The Data Protection Act 2018 governs the use of personal information by organizations, businesses, or the government in the UK.This Act represents the UK's adaptation of the General Data Protection Regulation (GDPR).All entities handling personal data are bound to adhere to stringent rules known as 'data protection principles'.

Be (cyber)secured :

Data Protection Impact Assessments

Iliomad’s expertise in conducting DPIAs for medical research can help you speed up your compliance program as well as benefit from iliomad’s unique templates and methodology.

Start assessing!

Due Diligence

iIliomad can assist you in thoroughly addressing all privacy-related requirements, ensuring that every necessary step has been taken to safeguard data. In the event of any privacy shortcomings, we can develop a detailed remediation plan to rectify these issues. Our expertise can play a vital role in securing a successful financing round and instilling confidence in your prospective financial partners.

Data Privacy Training

Mandatory GDPR training for all personnel involved in the processing of EU personal data is essential. Ensuring a consistent level of data protection across the entire company, from operational staff to management teams, is of utmost importance.

Train your team

Clinical Data Hosting

Hosting of clinical data has become a major concern for companies processing EU personal data. Iliomad can help you establish your hosting strategy and become compliant with hosting regulations

GDPR Quality Assurance

iliomad has crafted a bespoke and adaptable GDPR Quality Assurance (QA) system specifically designed for Life Sciences companies. This system is scalable, making it a suitable solution for everything from small biotech startups to large pharmaceutical corporations

In need of QA assistance?

Informed Consent Form Review

Informed Consent Forms are pivotal documents for clinical trials and privacy is now at the center of those documents. With its broad experience in the EU, iliomad can help speed up the process.

Let's be in touch!

GDPR Contractual Review

Iliomad has developed a broad experience within the life science industry to help every party abide with the GDPR and tackle the numerous correlated constraints.

Vendor Assessment

Vendors processing activities ranging from hosting patient data to data analysis must also comply with data privacy regulations. Iliomad can help you assess your vendors capabilities and measures to make sure your data is in good hands.

Gap Analysis: UK GDPR, HIPAA, PIPEDA & PIPL

We help our clients through gap analysis with the GDPR and other main privacy regulations. Iliomad has developed extensive expertise of the main privacy regulations of the world and can help you.

European Local Regulations

The General Data Protection Regulation (GDPR) is a regulation that aims to provide a consistent set of data protection rules across the European Union (EU). Although the GDPR is a European regulation, it allows EU member states to adapt certain provisions to better align with their national laws and practices. This can lead to nuances and variations in the way the rules are applied. Additionally each EU member state has its own regulator responsible for enforcing the GDPR. These authorities may have slightly different interpretations and different enforcement priorities.

UK Data Protection Act

The Data Protection Act 2018 governs the use of personal information by organizations, businesses, or the government in the UK.This Act represents the UK's adaptation of the General Data Protection Regulation (GDPR).All entities handling personal data are bound to adhere to stringent rules known as 'data protection principles'.

Be (cyber)secured :

UK Data Representative

In accordance with the UK General Data Protection Regulation (UK GDPR) and the Data Protection Act 2018, life sciences companies that are not established in the United Kingdom, but process the personal health data of individuals within the UK, are required to appoint a UK-based Data Protection Representative.

Drugs

Data protection has emerged as an essential aspect of managing clinical trials, and iliomad Health Data offers specialized guidance, drawing on extensive expertise in the nuances of privacy regulations as they apply to clinical research, to facilitate and assure compliance

Healthtech

In the Medtech sector, digital therapies, healthcare apps, and medical devices are all grounded in data collection and processing. As FDA and EMA regulations tighten, prioritizing data privacy in the development of these technologies is essential.

Data Warehouses

Data warehouses remove the barriers to the exploitation of medical data by enabling the collection and integration of massive health data. Iliomad supports you in obtaining regulatory approval for the creation of data warehouses.

AI Act

Artificial intelligence opens up enormous opportunities for healthcare. Iliomad can help companies take into consideration current and future privacy requirements in order to develop privacy compliant models.

Request our booklet

See how we can help you via our comprehensive program, set of tools and services.

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Contact us by email at contact@iliomad.fr

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