This privacy policy lays out how MedTrace Group consisting of MedTrace Pharma A/S, MedTrace AB and MedTrace Pharma, Inc., (in the following “MedTrace”) processes personal data on:
A. Identity and the contact details of the controller
Address:
B. Contact details of the Data Protection Officer
MedTrace is not obligated to designate a Data Protection officer, cf. Article 37 (1) GDPR, and has chosen not to appoint a Data Protection Officer.
C. Categories of personal data, purposes of the processing and the legal basis for the processing
Please note: Not all the information listed in a “Category of personal data” will necessarily be processed on the data subject in the corresponding “category of data subject”. In some circumstances, only some of the categories of personal data will be processed on the relevant data subject.
Category of data subject
Category of personal data per data subject
Visitors to website
Admins on our website
Data Subjects in our CRM system
Contact persons at suppliers, service providers, other contracting partners and research partners
Next of kin of MedTrace Employees
Members of the Board of Directors
Shareholders, investors, loan providers
Clinical trial subjects (MedTrace sponsored studies)
MedTrace uses a Data Processor, a “Contract Research Organization”, to perform the clinical trials. MedTrace will have no access to the information on the clinical trial subjects but seeing as MedTrace is the sponsor of the clinical trials, MedTrace is considered the Controller and thereby responsible for the protection of data.
Purpose of processing per data subject
Visitors to website
Admins on our website
Data subjects in our Customer Relationship Management system
Contact persons at suppliers, service providers, other contracting partners and research partners
Next of kin of MedTrace Employees
Members of the Board of Directors
Shareholders, investors, loan providers
Clinical trial subjects (MedTrace sponsored studies)
Legal basis for processing
Visitors to website
Admins on our website
Data subjects in our Customer Relationship Management system
Contact persons at suppliers, service providers, other contracting partners and research partners
Next of kin of MedTrace Employees
Members of the Board of Directors
Shareholders, investors, loan providers
Clinical trial subjects (MedTrace sponsored studies)
D. Consent
You can withdraw your consent to MedTrace’s processing of your personal data at any time. You can withdraw your consent by contacting us using the contact information provided above (section A).
The lawfulness of the processing and transfer based on your consent before your withdrawal is not affected if you choose to withdraw your consent. If you choose to withdraw your consent it will thus first have effect from this point of time.
E. Sources
The personal data we process on you is primarily provided directly from you or from your unit. In some cases, the information is provided from your employer or from public authorities such as tax authorities.
F. Provision and failure to provide
In most circumstances when we collect personal data directly from you, you provide us with the information voluntarily or in order to enter into or to fulfill the requirements of a contract with us. In some circumstances, you are obligated to provide the information to us, e.g. your personal identity/social security-number for reporting to the tax authorities.
The consequence of not providing the personal data, as listed above, is that we cannot address the purposes mentioned above. Thus, we cannot make the website available to you, we cannot communicate with you, we cannot comply with our obligations as your contracting party and cannot comply with our obligations towards public authorities.
G. Data Processors
MedTrace uses Data Processors to host personal data and to support our use of systems.
In relation to clinical trial subjects, MedTrace uses a Data Processor, Cardiovascular Clinical Studies located in Boston, USA, to manage the clinical trials (a “Contract Research Organizations” or “CRO”). The CRO will in many cases also use processors (e.g. “Principal Investigators”).
H. Transfer of personal data
In some cases, MedTrace transfers personal data to Data processors, to the MedTrace website, to public authorities or to external legal advisors and accountants.
I. Transfer to third countries
In some situations, MedTrace transfers personal data to countries outside of the EU/EEA countries, currently to the US. We transfer information to the US, because MedTrace has a US based department of MedTrace, MedTrace Pharma, Inc (US). In relation to clinical trials, MedTrace will transfer personal data to and from the US as the trials will take place in the US.
The Commission of the European Union has not made a decision on the legality of the practice on data protection in the US or the EU-US Privacy Shield. In most cases, transfers will be based on your consent, based on the necessity for the performance of a contract between you and MedTrace or based on the necessity for the performance of a contract in your interest between MedTrace and another natural or legal person, cf. art. 49 (1) (a), (b) and (c) GDPR.
J. Period of storage
Visitors on our website: Persistent cookies are stored for a period of up to 2 years and information on consent to cookies are stored for a period of up to 1 year.
Admins on our website: Persistent cookies are stored for a period of up to 2 years and information on admin settings are stored for a period of up to 1 year.
Data subjects in our CRM-system: We store personal data on you in our CRM-system until you ask to be deleted or until we have not had any interaction with you for more than five years.
Contact persons at contracting partners and research partners: We store personal data on you as long as it is relevant for our relationship, and as long as necessary to establish, determine or defend a legal claim.
Next of kin to MedTrace employees: We delete your personal data when the employee resigns.
Owners, members of management and members of the board of directors, members of the advisory board: We store personal data on you as long as it is relevant for our relationship, and as long as necessary to establish, determine or defend a legal claim.
Clinical trial subjects: Via our Data Processor, the CRO, we indirectly store personal data on you as long as necessary in order to address the purpose to which your personal data was collected. When determining how long we will store your personal data, we will consider (a) compliance with requirements to documentation according to legislation and (b) our opportunity to establish, determine or defend a legal claim.
K. Your rights
According to GPDR, you have the following rights (on those conditions and with the exceptions that follows from the regulation). If you wish to exercise any of the below-mentioned rights, you will need to contact us using the contact details provided above (section A).
L. Complaints
You also the right to complain to the Danish Data Protection Authority (in Danish: Datatilsynet), if you are dissatisfied with the way we process your personal data. You can find the contact details of the Danish Data Protection Authority on www.datatilsynet.dk.
M. Contact
Please do not hesitate to contact us if you have any questions in regard to the protection of your personal data or if you wish to exercise your legal rights. You can find the contact information above in section A.
N. Changes to this privacy notice
We reserve the right to change this privacy notice.
[Version: 22-11-2021]