Ensure regulatory compliance and business continuity with PRRC and DPO interim solutions tailored to your needs.
Interim Data Protection Officer services to meet DPO requirements under GDPR 2016/679
Interim PRRC for medical devices to meet MDR 2017/745 requirements
PRRC interim support per IVDR 2017/746
Management Representative role fulfilment per ISO 13485
Fulfilment of the Quality, Regulatory, and Information Security roles
As an organisation in the medical field, either developing, marketing or using medical devices, you may need to employ quality, regulatory, security and privacy personnel. As in many sectors, skilled & trained personnel are hard to get by, and you may need a temporary solution to fulfil a position.
We have a team of seasoned & experienced staff that can support your organisation on a temporary basis. Our PRRC and DPO interim solutions can assist in fulfilling the official European roles such as Data Protection Officer (DPO) required per the General Data Protection Regulation GDPR (2016/679) and the Person Responsible for Regulatory Compliance (PRRC), as required by the Medical Device Regulation – MDR (2017/745) and the In-Vitro Diagnostics Regulation – IVDR (2017/746). We can provide PRRC and DPO interim solutions with fractional QA, RA and Information Security support roles during start-up stages.
If a position needs to be temporarily filled with a broad scope of support or on a full-time basis, we aim to provide support by a wider team, to avoid a single staff member being employed on a full-time basis at a single organisation. This supports business continuity and a broader provision of expertise.
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Explore our blog posts on MDR, IVDR, and AI Act compliance to stay ahead of regulatory changes.
Find answers to common questions about our services, compliance processes, and how we can assist your business.
Interim support provides temporary access to qualified professionals who can fulfil regulatory, quality, privacy, security, or compliance responsibilities while organisations recruit permanent staff, manage periods of growth, or address resource shortages.
The PRRC is a role required under MDR (2017/745) and IVDR (2017/746). The PRRC is responsible for overseeing regulatory compliance activities, including technical documentation, conformity assessment procedures, post-market obligations, and regulatory reporting requirements.
Yes. MedQAIR can provide interim PRRC support to help organisations maintain compliance and business continuity while recruiting permanent personnel or addressing temporary resource gaps.
A Data Protection Officer supports organisations in meeting GDPR obligations related to personal data protection, privacy governance, risk management, training, and regulatory compliance. Certain organisations are legally required to appoint a DPO depending on their activities and processing operations.
Yes. MedQAIR can provide interim DPO support, helping organisations establish privacy governance processes, manage GDPR obligations, and maintain oversight of data protection activities during temporary staffing transitions.
Yes. Interim support can be provided on either a full-time or fractional basis depending on the organisation’s needs, workload, and regulatory obligations. This allows organisations to access expertise without requiring a full-time appointment.
Yes. Interim support can include quality management, regulatory affairs, information security, management representative responsibilities, and other compliance-related functions where temporary expertise is required.
Interim specialists help ensure that regulatory activities, quality processes, documentation reviews, audits, supplier oversight, post-market obligations, and compliance activities continue without interruption during staffing changes or periods of rapid growth.
Yes. Start-ups often require regulatory, quality, privacy, or security expertise before building a full internal team. Interim support provides access to experienced professionals while allowing organisations to scale resources according to their stage of development.
The deployment timeline depends on the required expertise, responsibilities, and scope of work. Interim support is often used when organisations need experienced resources more quickly than traditional recruitment processes allow.
Yes. Interim specialists can work alongside broader quality, regulatory, information security, privacy, or audit support activities to help organisations address both operational responsibilities and strategic compliance initiatives.
A team-based approach helps reduce dependency on a single individual and provides access to broader expertise across quality, regulatory, privacy, information security, and compliance domains. This can improve business continuity and resilience during periods of organisational change.
Yes. Interim specialists can assist with audit preparation, regulatory inspections, documentation reviews, compliance assessments, submission activities, and remediation programmes while maintaining day-to-day compliance responsibilities.
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