AdComplia is a Swiss based regulatory and medical affairs consultancy supporting ​pharmaceutical companies implement their global plans. Our solid expertise and broad range ​of services related to pharmaceutical advertising regulations and promotional review make us ​a trusted partner to guide your teams.

Our comprehensive knowledge of international and national regulations and codes governing the ​promotion of pharmaceuticals, coupled with a true understanding of scientific issues and business ​goals, enable AdComplia to provide customised guidance on the review and approval of your ​promotional and non-promotional materials. Our flexible and adaptable solutions ensure you ​remain at your most competitive in today’s complex and rapidly changing regulatory environment.

We provide services in the following areas:

• Regulatory review and approval of all advertising and promotional materials at global and ​regional level and in selected countries.
• Review of a full range of non-promotional commercial, medical, corporate, market access, ​policy, and training materials.
  
• Clear feedback on potential risks based on the local market, with a solution-oriented approach ​to finding compliant means to achieve the desired business objectives.
  
• Guidance on pre-approval communications.
  
• Training on material review and approval requirements.
  

• Support with set up, training and validation of compliance processes, including drafting and ​review of work instructions and standard operating procedures (SoPs).
• Adapting and streamlining the EDMS workflow for specific markets based on local requirements ​for review, approval, certification, and submission of promotional materials.
  
• Responsible Person for Drug Promotion in Switzerland.
  
• Our network of experts enables us to identify local responsible persons to review materials for ​compliance with national regulations and to submit to competent authorities in selected countries.
  

Our extensive experience in pre-clinical and clinical research throughout the drug development ​process across a range of therapeutic areas make AdComplia a preferred partner to guide ​planning and execution of your medical communications strategy.

Our services include:

• Medical review of the full rage of medical and commercial ​materials.
• Consulting on medical affairs and communication strategies.
  
• Third-party vendor management.
  
• Process management and setup.
  

Tell us how we can help and we'll create the best solutions for you.

Our clients range from small biotech companies in the pre-registration phase through to global ​pharmaceutical companies looking for interim or permanent support with review and final ​approval of promotional and non-promotional materials.

We seamlessly integrate into your team, providing full support to you and your marketing ​agencies from concept development through to implementation. We offer practical and ​pragmatic solutions to complex challenges with adaptability and flexibility designed to meet ​your evolving needs.

Ron Hogg, Director and Founder of AdComplia Sàrl

With a PhD in Pharmacology, and over 15 years of experience in the pharmaceutical industry, I specialize in ​regulatory compliance and medical communications. I have worked with global leaders including Takeda, Merck ​Serono, and Thermo Fisher, as well as biotech innovators such as Novavax and ALK, across diverse therapeutic ​areas including vaccines, rare diseases, hematology, immunology, neurology, and cardiology.

My experience covers medical/regulatory writing, medical communications, and regulatory affairs. I focus on ​partnering with Advertising and Promotion teams to guide the MLR review process. I review promotional and ​non-promotional materials and provide strategic advice on regulatory compliance ensuring that materials meet ​international and local regulations while aligning with commercial goals. My experience allows me to develop ​close and trusted partnerships with client and creative agency stakeholders, to deliver precise, actionable ​feedback based on local market considerations, and to offer alternative approaches to achieve the desired aims.

My international background as well as the diverse roles that I held over the past decades enable me to navigate ​the complexities of the pharmaceutical landscape, managing multiple projects and adapting to evolving priorities ​and tight deadlines.

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Find out how AdComplia can support your

regulatory compliance and medical affairs teams.