Navigate your pharmaceutical company safely through the regulatory maze

BAYOOCARE supports you in entering the medical device sector – from the approval strategy to ISO 13485 to the international market launch.

BAYOOCARE ist Legal Manufacturer as a Service, Legalhersteller für Medizinprodukte in über 30 Ländern
BAYOOCARE ist Legal Manufacturer as a Service, Legalhersteller für Medizinprodukte in über 30 Ländern

Navigate your MedTech company safely through the regulatory maze

BAYOOCARE supports you at every stage – from the initial product idea to MDR approval, market launch and beyond.

Your pharma-to-medical device journey

Pharma is heavily regulated – but medical devices according to MDR follow different rules. Instead of pharmacological proof of efficacy, the focus is on technical performance, clinical safety and ISO 13485-compliant quality management. BAYOOCARE accompanies you through this transition.

Our services for pharmaceutical companies

BAYOOCARE - Legal Manufacturer as a Service
  • Regulatory advice & approval

  • QMS according to ISO 13485

  • Clinical evaluation & trials

  • Risk management & conformity assessment

  • Post-Market Surveillance & Lifecycle

  • Market access & strategic consulting

  • Project management & operational support

  • Training & education

Still have questions? Please contact uswe know the answer.

Regulatory advice & approval

Tailor-made approval strategy for the MDR environment – with a focus on the differences to pharmaceutical approval. Technical documentation, risk analyses and communication with notified bodies.

QMS according to ISO 13485

Implementation or optimization of your QMS specifically for medical devices. Internal audits, supplier audits and training – even if a GMP system is already in place.

Clinical evaluation & trials

Planning and conducting clinical trials with a focus on technical performance and safety – instead of pharmacological proof of efficacy. Preparation of clinical evaluations and PMCF strategies.

Risk management & conformity assessment

Systematic risk management in accordance with ISO 14971: risk identification, assessment and minimization measures. Preparation and implementation of the conformity assessment for CE marking.

Post-Market Surveillance & Lifecycle

Development of PMS processes, creation of PSURs and vigilance activities. Change management and process optimization along the entire product life cycle.

Market access & strategic consulting

Market access strategies for the EU, CH, UK and USA, taking into account the special features of the medical device market. Advice on regulatory trends and country-specific requirements.

Project management & operational support

Project management for smooth development and approval processes. Resource planning, documentation support and coordination of all parties involved.

Training & education

Training on MDR/IVDR, ISO 13485, clinical evaluation and PMS for your teams – specially tailored to employees from the pharmaceutical sector who are new to the world of medical devices.

BAYOOCARE - Alfred Koch - CEO & PRRC

Alfred Koch

CEO | PRRC

How to contact us

Are you planning a project or do you have very specific regulatory questions about placing your medical device on the market? No matter what phase of your project you are in, we will be happy to support you. The quickest way to contact us – feel free to write to us.

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