About PharMarketing

Global Life Sciences Compliance Consulting Since 2013

PharMarketing is a specialized life sciences compliance consultancy helping pharmaceutical, biotechnology, medical device, clinical research organization (CRO), and healthcare companies meet complex regulatory, privacy, quality, and IT compliance requirements.


Founded in 2013 and headquartered in France, we support organizations operating across Europe, North America, Asia, Africa, and other international markets. Our mission is straightforward: to make compliance practical, proportionate, and operationally effective for organizations working in highly regulated life sciences environments.


Our 30+ team of multidisciplinary consultants combine expertise in data protection, clinical research, GxP quality systems, information technology, and regulatory compliance. We work alongside client teams to identify risks, strengthen governance, prepare for inspections, and embed sustainable compliance practices across the organization.


What Does PharMarketing Do?

PharMarketing provides practical consulting, advisory, audit, legal representation, training, and implementation support for life sciences organizations that need to manage regulatory obligations across jurisdictions.


We help clients with:

  • GDPR and global privacy compliance for clinical research and healthcare data
  • Data Protection Officer (DPO) and Data Protection Representative (DPR) services
  • EU, EEA, UK, and Switzerland legal representation
  • Clinical operations, vendor, quality-system, privacy, and IT compliance audits
  • Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Clinical Laboratory Practice (GCLP) support
  • Computerized System Validation (CSV) and regulated IT-system compliance
  • Compliance training for leadership, project teams, and end users


Our work is designed for organizations that need more than a theoretical interpretation of regulations. We translate requirements into action plans, controls, documentation, processes, and training that can work in the realities of clinical development, research operations, vendor management, and global commercialization.


Our Expertise:

GDPR and Privacy Compliance for Life Sciences

Life sciences organizations process sensitive personal data at every stage of research, development, clinical trials, pharmacovigilance, medical affairs, and commercial operations. PharMarketing helps companies establish and maintain privacy programs that reflect both GDPR requirements and the operational realities of regulated healthcare environments.


We understand that privacy compliance in clinical research must align with GCP, study protocols, ethics requirements, safety reporting, sponsor responsibilities, and cross-border data flows. Our approach connects legal and regulatory expectations with the people, systems, and processes responsible for executing clinical studies.


Why Life Sciences Organizations Choose PharMarketing


PharMarketing is built around the specific compliance challenges facing life sciences organizations. We recognize that a pharmaceutical sponsor, emerging biotech, global CRO, medical device company, or clinical-stage start-up does not need generic compliance advice. It needs guidance that reflects regulated processes, scientific timelines, patient-data responsibilities, vendor ecosystems, and international operating models.


Clients choose PharMarketing because we provide:

  • Life sciences specialization. Our work is focused on the regulatory, privacy, quality, and technology issues that affect life sciences organizations.
  • Global perspective. We support international operations and cross-border data flows involving Europe, North America, Asia, Africa, the UK, Switzerland, and other markets.
  • Operational solutions. We turn requirements into clear actions, practical documentation, governance structures, training, and improvement plans.
  • Risk-based thinking. We help teams focus resources on the risks that matter most to patients, data subjects, study integrity, product quality, and regulatory readiness.
  • Cross-functional expertise. We bridge privacy, legal, clinical operations, quality assurance, IT, cybersecurity, and validation considerations.
  • Flexible support. We work as advisors, auditors, trainers, outsourced privacy professionals, and extensions of internal compliance teams.


Who We Support

We work with organizations across the life sciences ecosystem, including:

  • Pharmaceutical companies
  • Biotechnology companies
  • Medical device manufacturers
  • In vitro diagnostic organizations
  • Clinical research organizations
  • Site management organizations
  • Laboratories and clinical laboratories
  • Digital health and health-tech companies
  • Healthcare organizations
  • Research institutions
  • Clinical-stage start-ups
  • Life sciences investors and acquirers conducting compliance due diligence
  • Technology providers serving regulated healthcare and research environments


Whether you are launching a clinical trial in Europe, expanding into a new market, selecting a technology provider, preparing for an inspection, responding to privacy requirements, or strengthening a mature compliance program, PharMarketing can help you move forward with greater clarity and confidence.


Frequently Asked Questions

What is PharMarketing?

PharMarketing is a life sciences compliance consultancy founded in 2013. We help pharmaceutical, biotech, medical device, CRO, healthcare, and related organizations manage GDPR, privacy, GxP, IT quality, CSV, audit, legal representation, training, and inspection-readiness requirements.


Where is PharMarketing based?

PharMarketing is headquartered in France and supports life sciences clients internationally, including organizations operating across Europe, North America, Asia, Africa, the UK, Switzerland, and the European Economic Area.pharmarketing


Does PharMarketing provide GDPR consulting for clinical trials?

Yes. PharMarketing supports GDPR and privacy compliance for clinical research and life sciences organizations, including privacy assessments, protocol and informed-consent reviews, data-transfer support, vendor oversight, DPIAs, governance, training, and representation services.


Can PharMarketing act as an external DPO?

Yes. PharMarketing provides external or part-time Data Protection Officer services, as well as Data Protection Representative support in the EU, EEA, UK, and Switzerland for eligible organizations.


Does PharMarketing support inspection readiness?

Yes. PharMarketing provides audit, quality, IT compliance, CSV, GxP, and inspection-readiness services to help life sciences organizations identify gaps, prepare evidence, address risks, and improve confidence ahead of regulatory inspections or partner audits.


Does PharMarketing work with early-stage biotech companies?

Yes. PharMarketing supports clinical-stage start-ups and growing life sciences companies, as well as established global organizations. Services can be tailored to the company’s stage of development, regulatory footprint, internal resources, clinical activity, and risk profile.


Talk to a Life Sciences Compliance Expert

Compliance challenges often sit at the intersection of privacy, clinical research, quality, IT, and international regulation. PharMarketing helps organizations address those challenges with expertise that is practical, risk-based, and grounded in life sciences operations.


Contact PharMarketing to discuss your life sciences compliance requirements.