We provide regulatory and quality consulting services throughout the entire product life-cycle.

When your company needs to define a regulatory strategy, create a dossier, or prepare for a FDA inspection or ISO audit, meditec Consulting brings in 20 years of experience in the pharmaceutical and device environment to support your project.
Our customers range from start-ups, SMEs to global players. We aim at providing you with a clear understanding of the requirements and support you with their efficient and practical implementation.

Service Types

meditec Consulting provides consulting services to the medical device,
pharmaceutical and healthcare industry. Our services include

• Regulatory Affairs
• Quality Management
• Risk Management
• Trainings and Seminars

Product Types

Our consultants have many years’ experience in European,
US and international regulations for

• Medical Devices
• In-vitro Diagnostics
• Combination Products
• Pharmaceuticals
• Biologics

Our Services

Monitoring changes to legislations, regulations and guidelines is complex and challenging in particular for small and medium enterprises. Outsourcing to experienced and specialized consultants on a project by project basis is an alternative to ensure that your internal team is managing its core business.

meditec Consulting is committed to develop customized services based on the specific needs of our clients. Our goal is to provide our clients with a clear understanding of the requirements they will encounter throughout the entire product lifecycle.